2-amino-quinoline derivatives

ABSTRACT

Described herein are 2-amino-quinoline derivatives that are agonists of toll-like receptors 7 and 8 (TLR7/8), pharmaceutical compositions, and methods of use of the compounds and compositions to treat various diseases, such as viral, cancer, and allergic diseases, in need thereof by administering a therapeutically effective amount of a 2-amino-quinoline derivative.

CROSS REFERENCE TO RELATED APPLICATIONS

This application is a division of U.S. patent application Ser. No. 16/608,581, filed Oct. 25, 2019, now U.S. Pat. No. ______, which is a 35 U.S.C. 371 national phase entry of PCT/CN2018/084674, filed Apr. 26, 2018, which claims the benefit of, and priority to, Chinese Patent Application Serial No. 201710287322.2, filed Apr. 27, 2017, the entire disclosures of which are each hereby incorporated by reference in their entireties.

FIELD OF THE INVENTION

The present invention relates to 2-amino-quinoline derivatives, such as imidazoquinoline and pyrazoloquinoline analogs as agonists of toll-like receptors 7 and 8 (TLR7 and TLR8), as well as pharmaceutical compositions comprising the same. The present invention also relates to the use of the compounds, compositions, and the method of activating TLR7 and TLR8 in treating various diseases.

BACKGROUND OF THE INVENTION

The TLR family plays a fundamental role in pathogen recognition and activation of innate immunity. TLR7 and TLR8 are toll-like receptors 7 and 8 respectively, and they lie in close proximity to each other on the human X chromosome. Both TLR7 and TLR8 recognize single-stranded RNA of viruses such as HIV and HCV. TLR7 has been shown to play a significant role in the pathogenesis of autoimmune disorders such as Systemic Lupus Erythematosus (SLE) as well as in the regulation of antiviral immunity. Genetic variants in TLR8 have recently been linked to susceptibility to pulmonary tuberculosis. TLR7 is functional both in human and mouse, while TLR8 is only functional in human, but it seems to counteract TLR7 activity. The major benefit of TLR7/8 agonists as immune response enhancers is their simultaneous stimulation of several cell types. TLR7 and TLR8 are expressed mostly on immune cells such as antigen presenting cells, including plasmacytoid dendritic cells (pDC) and myeloid dendritic cells (mDC), as well as natural killer cells, and macrophages. Activation of TLR7/8 on pDCs and mDCs results in the induction and release of type I interferons (IFN), tumor necrosis factor alpha (TNFα), and interleukin 12 (IL-12), which is an important step for the initiation of innate and adaptive immunities to kill cancer cells. For these reasons, TLR7 and TLR8 have become interesting targets in both antiviral and cancer therapy. There is also a growing interest in the targeting of toll-like receptors, such as TLR7/8 for the treatment of allergic diseases.

Small molecule agonists at TLR7 and TLR8 have increased interest in both antiviral and cancer research own to their profound antiviral and antitumor activity. The lead compound of the imidazoquinoline family, imiquimod, is efficacious against many primary skin tumors and cutaneous metastases and is marketed as a topical formulation. Resiquimod (R-848), from the same imidazoquinoline family, is a low molecular weight synthetic molecule that activates immune cells via the TLR7/TLR8 MyD88-dependent signaling pathway. It acts as an immune response modifier and has antiviral and antitumor activity. It has several mechanisms of action, being both an agonist for toll-like receptors 7 and 8, and an upregulator of the opioid growth factor receptor. R-848 is used as a topical gel in the treatment of skin lesions such as those caused by the herpes simplex virus and cutaneous T cell lymphoma, as an adjuvant to increase the effectiveness of vaccines, and as an adjuvant to immunotherapy in allergic rhinitis (AR) patient. Therefore, in addition to their use as stand-alone immunotherapeutic agent, TLR7/8 agonists hold promise as adjuvants in cancer vaccine or adoptive T cell transfer protocols. Extension of the families of the known synthetic TLR7/8 agonists, such as described above, pave the way to the development and identification of TLR7/8 agonists that are well tolerated, more selective with potent antitumor and antiviral activity, broadly applicable, and more effective as adjuvants.

SUMMARY OF THE INVENTION

Described herein are 2-amino-quinoline derivatives, pharmaceutically acceptable salts, solvates, prodrug and active metabolites, that are agonists of toll-like receptors 7 and 8 (TLR7/8). These compounds may be used to treat viral infection, such as HCV, cancer, and allergic diseases in need thereof by administering a therapeutically effective amount of a 2-amino-quinoline derivative.

Some embodiments include a compound represented by Formula 1:

wherein a dashed line represents the presence or absence of a bond; A¹ is CR¹, NR^(1A), or N; A² is CR², NR^(2A), O, or S; B¹ is CR⁵ or N; B² is CR⁶ or N; B³ is CR⁷ or N; R^(I) and R² are independently F, Cl, Br, I, NO₂, CN, R^(a), —OR^(a), —NR^(a)R^(b), —NHCOR^(a), —NHSO₂R^(a), —OCOR^(a), or —SO₂R^(a); X is a bond, O, NR^(a), —CO—, —SO—, or —SO₂—, —CONR^(a), hydrocarbyl, and R³ is H or C₁₋₃₀ organyl; or X-R³ is F or Cl; R^(1A), R^(2A), R⁴, R^(a), and R^(b) are independently H or C₁₋₃₀ organyl; R⁵, R⁶, and R⁷ are independently F, Cl, Br, I, NO₂, CN, R^(a), —OR^(a), —NR^(a)R^(b), —NHCOR^(a), —NHSO₂R^(a), —OCOR^(a), —SO₂R^(a), —SO₂NHR^(a), or —X¹—(C_(m)H_(2m)O₀₋₁)—Z—(C_(n)H_(2n+1)), —(C_(m)H_(2m)O₀₋₁)—Z—(C_(n)H_(2n+1)), wherein R⁵ and R⁶ or R⁶ and R⁷ can be optionally linked to form a ring; wherein X¹ is a bond, O, NR^(a), —CO—, —SO—, or —SO₂—; Z is a bond, O, NHSO₂, or NHCO; m is 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10; and n is 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, or 23.

Some embodiments include a pharmaceutical dosage form comprising a subject compound. A subject compound or a subject composition may be used for activating TLR7/8. In addition to its use as a stand-alone immunotherapeutic agent, such as an antiviral and anticancer agent, a subject compound or composition may be used as adjuvants in cancer vaccine or adoptive T cell transfer protocols.

Some embodiments include a method of treating a disease or disorder associated with a TLR7/8 agonist comprising administering an effective amount of a subject compound to a mammal in need thereof

Some embodiments include use of a subject compound in the manufacture of a medicament for the treatment of a disease or disorder associated with a TLR7/8 agonist.

DETAILED DESCRIPTION OF THE INVENTION

Unless otherwise indicated, when a compound or chemical structural feature, such as alkyl, alkenyl, alkynyl, aryl, heteroaryl, etc., is referred to as being “optionally substituted,” it includes a feature that has no substituents (i.e. unsubstituted), or a feature that is “substituted,” meaning that the feature has one or more substituents. The term “substituent” has the broadest meaning known to one of ordinary skill in the art, and includes a moiety that occupies a position normally occupied by one or more hydrogen atoms attached to a parent compound or structural feature. In some embodiments, a substituent may be an ordinary organic moiety known in the art, which may have a molecular weight (e.g. the sum of the atomic masses of the atoms of the substituent) of 15-50 g/mol, 15-100 g/mol, 15-150 g/mol, 15-200 g/mol, 15-300 g/mol, or 15-500 g/mol. In some embodiments, a substituent comprises, or consists of: 0-30, 0-20, 0-10, or 0-5 carbon atoms; and 0-30, 0-20, 0-10, or 0-5 heteroatoms, wherein each heteroatom may independently be: N, O, S, Si, F, Cl, Br, or I; provided that the substituent includes one C, N, O, S, Si, F, Cl, Br, or I atom. Examples of substituents include, but are not limited to, alkyl, alkenyl, alkynyl, heteroalkyl, aryl, heteroaryl, hydroxy, alkoxy, aryloxy, acyl, acyloxy, alkylcarboxylate, thiol, alkylthio, cyano, halo, thiocarbonyl, O-carbamyl, N-carbamyl, O-thiocarbamyl, N-thiocarbamyl, C-amido, N-amido, S-sulfonamido, N-sulfonamido, isocyanato, thiocyanato, isothiocyanato, nitro, silyl, sulfenyl, sulfinyl, sulfonyl, haloalkyl, haloalkoxyl, trihalomethanesulfonyl, trihalomethanesulfonamido, amino, etc.

For convenience, the term “molecular weight” is used with respect to a moiety or part of a molecule to indicate the sum of the atomic masses of the atoms in the moiety or part of a molecule, even though it may not be a complete molecule.

As used herein, the term “alkyl” has the broadest meaning generally understood in the art and may include a moiety composed of carbon and hydrogen containing no double or triple bonds. Alkyl may be linear alkyl, branched alkyl, cycloalkyl, or a combination thereof and in some embodiments, may contain from one to thirty-five carbon atoms. In some embodiments, alkyl may include C₁₋₁₀ linear alkyl, such as methyl (—CH₃), methylene (—CH₂—), ethyl (—CH₂CH₃), ethylene (—C₂H₄—), propylene (—C₃CH₆—), n-butyl (—CH₂CH₂CH₂CH₃), n-pentyl (—CH₂CH₂CH₂CH₂CH₃), n-hexyl (—CH₂CH₂CH₂CH₂CH₂CH₃), etc.; C₃₋₁₀ branched alkyl, such as C₃H₇ (e.g. iso-propyl), C₄H₉ (e.g. branched butyl isomers), C₅H₁₁ (e.g. branched pentyl isomers), C₆H₁₃ (e.g. branched hexyl isomers), C₇H₁₅ (e.g. heptyl isomers), etc.; C₃₋₁₀ cycloalkyl, such as C₃H₅ (e.g. cyclopropyl), C₄H₇ (e.g. cyclobutyl isomers such as cyclobutyl, methylcyclopropyl, etc.), C₅H₉ (e.g. cyclopentyl isomers such as cyclopentyl, methylcyclobutyl, dimethylcyclopropyl, etc.) C₆H₁₁ (e.g. cyclohexyl isomers), C₇H₁₃ (e.g. cycloheptyl isomers), etc.; and the like.

As used herein the term “aryl” includes a group that can be derived from a monocyclic and polycyclic aromatic hydrocarbon by removal of a hydrogen atom from a ring carbon atom. The “aryl” may include an aromatic ring or aromatic ring system such as phenyl, naphthyl, etc.

The term “heteroaryl” has the broadest meaning understood by a person of ordinary skill in the art and includes an “aryl” which has one or more heteroatoms in the ring or ring system, such as pyridinyl, furyl, thienyl, oxazolyl, thiazolyl, imidazolyl, triazolyl, oxadiazolyl, isoxazolyl, indolyl, quinolinyl, benzofuranyl, benzothienyl, benzooxazolyl, benzothiazolyl, benzoimidazolyl, etc.

Unless otherwise indicated, any reference to a compound herein by structure, name, or any other means includes pharmaceutically acceptable salts, such as HCl, HBr, HI, H₂SO₄, acetate, citrate, phosphate, sodium, potassium, and ammonium salts; prodrugs, such as ester prodrugs; alternate solid forms, such as polymorphs, solvates, hydrates, etc.; tautomers; or any other chemical species that may rapidly convert to a compound described herein under conditions in which the compounds are used as described.

If stereochemistry is not indicated, a name or structural representation includes any stereoisomer or any mixture of stereoisomers.

For the purposes of this disclosure, “treat,” “treating,” or “treatment” includes use of a compound, composition, therapeutically active agent, or drug in the diagnosis, cure, mitigation, treatment, or prevention of disease or other undesirable condition.

With respect to any relevant structural representation, such as Formula 1, a dashed line represents the presence or absence of a bond. For example, compounds represented by Formulas 1A and 1B are included.

With respect to any relevant structural representation, such as Formula 1, 1A, or 1B, A¹ is CR¹, NR^(1A), or N. In some embodiments, A¹ is CW. In some embodiments, A¹ is NR^(1A). In some embodiment, A¹ is N.

With respect to any relevant structural representation, such as Formula 1, 1A, or 1B A² is CR², NR^(2A), O, or S. In some embodiments, A² is CR². In some embodiments, A² is NR^(2A). In some embodiments, A² is O. In some embodiments, A² is S.

With respect to any relevant structural representation, such as Formula 1, 1A, or 1B, X is a bond, O, NR^(a), —C(═O)—, —S(═O)—, —S(═O)₂—, —CONR^(a), hydrocarbyl, and R³ is H or C₁₋₃₀ organyl; or X-R³ is F or Cl. In some embodiments, X is a bond. In some embodiments, X is O. In some embodiments, X is NR^(a). In some embodiments, X is —C(═O)—. In some embodiments, X is —S(═O)—. In some embodiments, X is —S(═O)₂—. In some embodiments, X-R³ is F. In some embodiment, X-R³is Cl.

With respect to any relevant structural representation, such as R^(a), NR^(a), —OR^(a), —OCOR^(a), or —SO₂R^(a), —NR^(a)R^(b), in such as Formula 1, 1A or 1B, R^(a) or R^(b) is independently H or organyl, such as C₁₋₃₀ organyl, including any organic substituent group, regardless of functional type, having a free valence at a carbon, such as optionally substituted alkyl, e.g. optionally substituted C₁₋₃₀, C₁₋₁₂, C₁₋₆, or C₁₋₃ alkyl, including methyl, ethyl, C₃ alkyl, C₄ alkyl, C₅ alkyl, C₆ alkyl, C₇ alkyl, C₈ alkyl, C₉ alkyl, C₁₀ alkyl, C₁₁ alkyl, C₁₂ alkyl, C₁₃ alkyl, C₁₄ alkyl, C₁₅ alkyl, C₁₆ alkyl, C₁₇ alkyl, C₁₈ alkyl, C₁₉ alkyl, C₂₀ alkyl, C₂₁ alkyl, C₂₂ alkyl, C₂₃ alkyl, C₂₄ alkyl, C₂₅ alkyl, C₂₆ alkyl, C₂₇ alkyl, C₂₈ alkyl, C₂₉ alkyl, C₃₀ alkyl, C₃ cycloalkyl, C₄ cycloalkyl, C₅ cycloalkyl, C₆ cycloalkyl, C₇ cycloalkyl, C₈ cycloalkyl, C₉ cycloalkyl, C₁₀ cycloalkyl, C₁₁ cycloalkyl, C₁₂ cycloalkyl, etc.; optionally substituted alkenyl, e.g. optionally substituted C₂₋₁₂ or C₂₋₆, alkenyl, including ethenyl, C₃ alkenyl, C₄ alkenyl, C₅ alkenyl, C₆ alkenyl, C₇ alkenyl, C₈ alkenyl, C₉ alkenyl, C₁₀ alkenyl, C₁₁ alkenyl, C₁₂ alkenyl, C₄ cycloalkenyl, C₅ cycloalkenyl, C₆ cycloalkenyl, C₇ cycloalkenyl, C₈ cycloalkenyl, C₉ cycloalkenyl, C₁₀ cycloalkenyl, C₁₁ cycloalkenyl, C₁₂ cycloalkenyl, etc.; optionally substituted alkynyl, e.g. optionally substituted C₂₋₁₂ or C₂₋₆ alkynyl, including ethynyl, C₃ alkynyl, C₄ alkynyl, C₅ alkynyl, C₆ alkynyl, C₇ alkynyl, C₈ alkynyl, C₉ alkynyl, C₁₀ alkynyl, C₁₁ alkynyl, C₁₂ alkynyl, C₅ cycloalkynyl, C₆ cycloalkynyl, C₇ cycloalkynyl, C₈ cycloalkynyl, C₉ cycloalkynyl, cycloalkynyl, C₁₁ cycloalkynyl, C₁₂ cycloalkynyl, etc.; optionally substituted aryl, such as optionally substituted phenyl, optionally substituted naphthyl, etc.; optionally substituted heterocyclyl, optionally substituted heteroaryl, etc.; organyl also includes CN, —C(O)R^(a), —C(O)OR^(a), —C(O)NHR^(a), —C(O)NR^(a)R^(b), —C(O)—Z-organyl, wherein Z is a bond, O, S, or NR^(a)R^(b), —C(R^(a)R^(b))—OR^(a), —C(R^(a)R^(b))—NR^(a)R^(b). In some embodiments, R^(a) or R^(b) is independently H or C₁₋₃₀ hydrocarbyl, such as alkyl, alkenyl, alkynyl, or phenyl. In some embodiments, C₁₋₃₀ organyl can be substituted by halogen, hydroxyl, amines, alkoxyl, aryl, heteroaryl, sulfone, sulfonamide, carboxylic acid, amide, reversed amide, ester, cycloalkyl, heterocycloalkyl, carbonyl, alkyl, alkenyl, alkynyl, phosphonamidic acid, phosphinic amide, or phosphine oxide.

Some embodiments include a compound of Formula 2 or Formula 2A.

With respect to any relevant structural representation, such as Formula 1, 1A, 1B, 2, or 2A, B¹ is CR⁵ or N. In some embodiments, B¹ is CR⁵. In some embodiments, B¹ is N.

With respect to any relevant structural representation, such as Formula 1, 1A, 1B, 2, or 2A, B² is CR⁶ or N. In some embodiments, B² is CR⁶. In some embodiments, B² is N.

With respect to any relevant structural representation, such as Formula 1, 1A, 1B, 2, or 2A, B³ is CR⁷ or N. In some embodiments, B³ is CR⁷. In some embodiments, B³ is N.

Some embodiments include a compound of Formula 3A, 3B, 3C, 3D, 3E, 4, 5, 6, 7, 8, 9, 10, 11, 12, or 13.

With respect to any relevant structural representation, such as Formula 1, 1A, 1B, 2, 2A, 3A, 3B, 3C, 3D, 3E, 4, 5, 6, 7, 8, 9, 10, 11, 12, or 13, R¹ or R^(1A) is independently H or any substituent, such as F, Cl, Br, I, NO₂, CN, R^(a), —NR^(a)R^(b), —NHCOR^(a), —NHSO₂R^(a), —OCOR^(a), or —SO₂R^(a). In some embodiments, R¹ or R^(1A) is C_(r)H₂₊₁O, wherein r is 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10, including C₂H₅O, such as —(CH₂)₂OH; C₃H₇O, such as —CH₂OCH₂CH₃, —(CH₂)₂OCH₃, etc.; C₁₋₁₂ alkyl, such as —(CH₂)₃CH₃, —CH₂CH₂CH(CH₃)₂.

In some embodiments, R¹ or R^(1A) is —(CH₂)₂OH. In some embodiments, R¹ or R^(1A) is —CH₂OCH₂CH₃. In some embodiments, R¹ or R^(1A) is —(CH₂)₂OCH₃. In some embodiments, R¹ or R^(1A) is —(CH₂)₃CH₃ In some embodiments, R¹ or R^(1A) is —CH₂CH₂CH(CH₃)₂.

With respect to any relevant structural representation, such as Formula 1, 1A, 1B, 2, 2A, 3A, 3B, 4, 5, 6, 7, 8, 9, or 10, R² or R^(2A) is independently H or any substituent, such as —CH₃, —CH₂CH(CH₃)₂, —CH₂C(CH₃)₂R⁸, —CH₂CH₂C(CH₃)₂R⁸, —C₄H₉O, —CH₂CH₂OCH(CH₃)₂.

In some embodiments, R² or R^(2A) is H. In some embodiments, R² or R^(2A) is CH₃. In some embodiments, R² or R^(2A) is —CH₂CH(CH₃)₂. In some embodiments, R² or R^(2A) is —CH₂C(CH₃)₂R⁸. In some embodiments, R² or R^(2A) is —CH₂C(CH₃)₂OH. In some embodiments, R² or R^(2A) is —CH₂CH₂C(CH₃)₂OH. In some embodiments, R² or R^(2A) is —CH₂CH₂OCH(CH₃)₂.

With respect to any relevant structural representation, such as Formula 1, 1A, 1B, 2, 2A, 3A, 3B, 3C, 3D, 4, 5, 6, 7, 8, 9, or 10, R³ is any substituent, such as C₁₋₃₀ optionally substituted alkyl, —C_(w)H_(2w+1)O or an ester thereof, wherein w is 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10; —(C_(u)H_(2u)O₀₋₁)—Z—(C_(v)H_(2v+1)), wherein Z is a bond, O, NHSO₂, or NHCO, u is 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10, and v is 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, or 24; or —(C_(t)H_(2t)O₀₋₁)—Ht, wherein t is 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, or 20, and Ht is optionally substituted C₃₋₁₀ heterocyclyl.

In some embodiments, R³ is H. In some embodiment, R³ is CH₃. In some embodiments, R³ is —CH₂CH(CH₃)₂ In some embodiments, R³ is —(CH₂)₂CH(CH₃)₂ In some embodiments, R³ is —CH₂CH(OH)CH₃. In some embodiments, R³ is —(CH₂)₂CH(OH)CH₃. In some embodiments, R³ is —(CH₂)₂C(CH₃)₂OH. In some embodiments, R³ is (CH₂)₂OCH(CH₃)₂, —(CH₂)₃NHSO₂CH₃, —(CH₂)₄NHSO₂CH₃, —(CH₂)₂O(CH₂)₂NHSO₂CH₃, —(CH₂)₃NHCOC₁₇H₃₅, —(CH₂)₃NHCOCH₃, —(CH₂)₄NHCOCH₃, —(CH₂)₄NHCOC₁₇H₃₅, —(CH₂)₃NH₂,

With respect to any relevant structural representation, such as Formula 3E, R³ is C₁₋₃ alkyl optionally substituted with 1 to 6 of R^(8A), same or different, wherein R^(8A) is OH, oxide, C₁₋₆ organyl, or —O— (C₁₋₆ organyl).

With respect to any relevant structural representation, such as Formula 1, 1A, 1B, 2, 2A, 3A, 3B, 3C, 3D, 3E, 4, 5, 6, 7, 8, 9, 10, 11, 12, or 13, R⁴ is H or any substituent, such as hydrocarbyl.

In some embodiments, R⁴ is H.

With respect to any relevant structural representation, such as Formula 1, 1A, 1B, 2, 2A, 3A, 3B, 3C, 3D, 3E, 4, 5, 6, 7, 8, 9, 10, 11, 12, or 13, R⁵ is H or any substituent, such as F, Cl, R^(a), —CO₂R^(a), —CONR^(a)R^(b), CN, —OR^(a), −NR^(a)R^(b), —NHCOR¹, NHSO₂R^(a), —OCOR^(a), or —SO₂R^(a), wherein R^(a) and R^(b) are independently H or C₁₋₃₀ organyl. In some embodiments, R⁵ is —(C_(m) H_(2m)O₀₋₁)—Z—(C_(n)H_(2n+1)), wherein Z is a bond, O, —NHSO₂, or —NHCO, m is 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10, and n is 1, 2, 3, 4, 5, 6. 7. 8. 9. 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, or 24. In some embodiments, R⁵ is H.

With respect to any relevant structural representation, such as Formula 1, 1A, 1B, 2, 2A, 3A, 3B, 3C, 3D, 3E, 4, 5, 6, 7, 8, 9, 10, 11, 12, or 13, R⁶ is H or any substituent, such as F, Cl, R^(a), —CO₂R^(a), —CONR^(a)R^(b), CN, —OR^(a), —NR^(a)R^(b), —NHCOR^(a), —NHSO₂R^(a), —OCOR^(a), or —SO₂R^(a), wherein R^(a) and R^(b) are independently H or C₁₋₃₀ organyl. In some embodiment, R⁶ is —(C_(m)H_(2m)O₀₋₁)—Z—(C_(n)H_(2n+1)), wherein Z is a bond, O, —NHSO₂, or —NHCO, m is 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10, and n is 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, or 24. In some embodiments, R⁶ is H.

With respect to any relevant structural representation, such as Formula 1, 1A, 1B, 2, 2A, 3A, 3B, 3C, 3D, 3E, 4, 5, 6, 7, 8, 9, 10, 11, 12, or 13, R⁷ is H or any substituent, such as F, Cl, R^(a), —CO₂R^(a), —CONR^(a)R^(b), CN, —OR^(a), —NR^(a)R^(b), —NHCOR^(a), —NHSO₂R^(a), —OCOR^(a), or —SO₂R^(a), wherein R^(a) and R^(b) are independently H or C₁₋₃₀ organyl. In some embodiment, R⁷ is —(C_(m)H_(2m)O₀₋₁)—Z—(C_(n)H_(2n+1)), wherein Z is a bond, O, —NHSO₂, or —NHCO, m is 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10, and n is 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, or 24. In some embodiments, R⁷ is H.

With respect to any relevant structural representation, such as Formula 4, 5, 6, 7, 8, 9, or 10, R⁸ is H, OH or C₁₋₆ alkyl. In some embodiments, R⁸ is H. In some embodiments, R⁸ is OH. In some embodiment, R⁸ is CH₃.

With respect to any relevant structural representation, such as Formula 3E, R^(8A) is OH, oxide, C₁₋₆ organyl, or —O—(C₁₋₆ organyl). 1 to 6, same or different R^(8A) can be attached at any ring C-atom. In some embodiments, R^(8A) is OH. In some embodiments, R^(8A) is CH₃. In some embodiments, two different R^(8A), such as CH₃ and OH, are attached to a same ring C-atom. In some embodiments, R^(8A) is —C(CH₃)₂OH.

With respect to any relevant structural representation, such as Formula 1, 1A, 1B, 2, 2A, 3A, 3B, 3C, 3D, 4, 5, 6, 7, 8, 9, or 10, in some embodiment, R³ and R⁴ are independently H or C₁₋₁₂ organyl; R′, R², R⁵, R⁶, and R⁷ are independently F, Cl, Br, I, NO₂, CN, —OR^(a), —NR^(a)R^(b), —OCOR^(a), or —SO₂R^(a); R^(1A) and R^(2A) are R^(a); R^(a) and R^(b) are independently H or C₁₋₁₂ organyl; and R⁸ is H or OH. In some embodiment, R⁵ and R⁶ or R⁶ and R⁷ can be optionally linked to form a saturated or an unsaturated ring.

Some embodiments include optionally substituted 9-methoxy-1H-imidazo [4,5-c]quinolin-4-amine or a salt thereof.

Some embodiments include optionally substituted 1-(4-amino-2-(ethoxymethyl)-9-methoxy-1H-imidazo[4,5-c]quinolin-1-yl)-2-methylpropan-2-ol or a salt thereof; optionally substituted 2-(ethoxymethyl)-1-isobutyl-9-methoxy-1H-imidazo[4,5-c]quinolin-4-amine or a salt thereof; optionally substituted 1 -(4-amino-9-methoxy-2-(2-methoxyethyl)-1H-imidazo[4,5 -c]quinolin-1-yl)-2-methylpropan-2-ol or a salt thereof; optionally substituted 1-(4-amino-2-(2-hydroxyethyl)-9-methoxy-1H-imidazo[4,5-c]quinolin-1-yl)-2-methylpropan-2-ol or a salt thereof; optionally substituted 4-((4-amino-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-9-yl)oxy)-2-methylbutan-2-ol or a salt thereof; optionally substituted 2-(ethoxymethyl)-9-(isopentyloxy)-1H-imidazo[4,5-c]quinolin-4-amine or a salt thereof; optionally substituted 4-((4-amino-2-(ethoxymethyl)-1H-imidazo[4,5 -c]quinolin-9-yl)oxy)butan-2-ol or a salt thereof; optionally substituted 1-((4-amino-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-9-yl)oxy)propan-2-ol or a salt thereof; optionally substituted 4-((4-amino-2-(2-methoxyethyl)-1H-imidazo[4,5-c]quinolin-9-yl)oxy)-2-methylbutan-2-ol or a salt thereof; optionally substituted 4-((4-amino-2-(ethoxymethyl)-1-methyl-1H-imidazo[4,5-c]quinolin-9-yl)oxy)-2-methylbutan-2-ol or a salt thereof; optionally substituted 2-(ethoxymethyl)-9-(2-isopropoxyethoxy)-1H-imidazo[4,5-c]quinolin-4-amine or a salt thereof; or optionally substituted 4-((4-amino-2-(ethoxymethyl)-1-isobutyl-1H-imidazo[4,5-c]quinolin-9-yl)oxy)-2-methylbutan-2-ol or a salt thereof; optionally substituted 2-(ethoxymethyl)-1-(2-isopropoxyethyl)-9-methoxy-1H-imidazo[4,5-c]quinolin-4-amine or a salt thereof; optinoally substituted 4-(4-amino-2-(ethoxymethyl)-9-methoxy-1H-imidazo[4,5-c]quinolin-1-yl)-2-methylbutan-2-ol or a salt thereof; optionally substituted 2-(ethoxymethyl)-9-isobutoxy-1H-imidazo[4,5-c]quinolin-4-amine or a salt thereof; optionally substituted 2-(ethoxymethyl)-9-(2-isopropoxyethoxy)-1-methyl-1H-imidazo[4,5-c]quinolin-4-amine or a salt thereof; optionally substituted 2-(ethoxymethyl)-9-(isopentyloxy)-1-methyl-1H-imidazo[4,5-c]quinolin-4-amine or a salt thereof; optionally substituted 2-(ethoxymethyl)-9-isobutoxy-1-methyl-1H-imidazo[4,5-c]quinolin-4-amine or a salt thereof; optionally substituted N-(3-((4-amino-2-(ethoxymethyl)-1-methyl-1H-imidazo[4,5-c]quinolin-9-yl)oxy)propyl)methanesulfonamide or a salt thereof; optionally substituted N-(2-(2-((4-amino-2-(ethoxymethyl)-1-methyl-1H-imidazo[4,5-c]quinolin-9-yl)oxy)ethoxy)ethyl)-methanesulfonamide or a salt thereof; optionally substituted N-(3-((4-amino-2-(ethoxymethyl)-1-methyl-1H-imidazo[4,5-c]quinolin-9-yl)oxy)propyl)acetamide or a salt thereof; optionally substituted N-(4-((4-amino-2-(ethoxymethyl)-1-methyl-1H-imidazo[4,5-c]quinolin-9-yl)oxy)butyl)methanesulfonamide or a salt thereof; optionally substituted N-(3-((4-amino-2-(ethoxymethyl)-1-methyl-1H-imidazo[4,5-c]quinolin-9-yl)oxy)propyl)stearamide or a salt thereof; optionally substituted N-(4-((4-amino-2-(ethoxymethyl)-1-methyl-1H-imidazo[4,5-c]quinolin-9-yl)oxy)butypacetamide or a salt thereof; optionally substituted N-(4-((4-amino-2-(ethoxymethyl)-1-methyl-1H-imidazo[4,5-c]quinolin-9-yl)oxy)butyl)-stearamide or a salt thereof; optionally substituted 2-(ethoxymethyl)-1-methyl-9-(2-morpholinoethoxy)-1H-imidazo[4,5-c]quinolin-4-amine or a salt thereof; optionally substituted 2-(ethoxymethyl)-1-methyl-9-((tetrahydrofuran-3-yl)oxy)-1H-imidazo[4,5-c]quinolin-4-amine or a salt thereof; optionally substituted 2-(ethoxymethyl)-1-methyl-9-(pyrrolidin-3-yl)oxy)-1H-imidazo[4,5-c]quinolin-4-amine or a salt thereof; optionally substituted 2-(ethoxymethyl)-1-methyl-9-(piperidin-4-yl)oxy)-1H-imidazo[4,5-c]quinolin-4-amine or a salt thereof; optionally substituted N-(3-((4-amino-2-(ethoxymethyl)-1-methyl-1H-imidazo[4,5-c]quinolin-9-yl)oxy)propyl)palmitamide or a salt thereof; optionally substituted N-(4-((4-amino-2-(ethoxymethyl)-1-methyl-1H-imidazo[4,5-c]quinolin-9-yl)oxy)butyl)palmitamide or a salt thereof; optionally substituted 9-(3-aminopropoxy)-2-(ethoxymethyl)-1-methyl-1H-imidazo[4,5-c]quinolin-4-amine or a salt thereof; optionally substituted 2-(ethoxymethyl)-9-isopropoxy-1-methyl-1H-imidazo[4,5-c]quinolin-4-amine or a salt thereof; optionally substituted 1-((4-amino-2-(ethoxymethyl)-1-methyl-1H-imidazo [4,5-c]quinolin-9-yl)oxy)-2-methylpropan-2-ol or a salt thereof; optionally substituted 2-(ethoxymethyl)-3,4-dihydro-5-oxa-1,2a,9-triazanaphtho[2,1,8-cde]azulen-10-amine or a salt thereof; optionally substituted (R)-2-(10-amino-2-(ethoxymethyl)-3,4-dihydro-5-oxa-1,2a,9-triazanaphtho[2,1,8-cde]azulen-3-yl)propan-2-ol or a salt thereof; optionally substituted (S)-2-(10-amino-2-(ethoxymethyl)-3,4-dihydro-5-oxa-1,2a,9-triazanaphtho[2,1,8-cde]azulen-3-yl)propan-2-ol or a salt thereof; optionally substituted (S)-2-amino-12-(ethoxymethyl)-6-methyl-6,7dihydro-5H-3,4-(azenometheno)[1,5]oxazocino[4,3,2-de]quinolin-6-ol or a salt thereof; optionally substituted (R)-2-amino-12-(ethoxymethyl)-6-methyl-6,7-dihydro-5H-3,4-(azenometheno)[1,5]oxazocino[4,3,2-de]quinolin-6-ol or a salt thereof; optionally substituted (R)-2-amino-12-(ethoxymethyl)-6,7-dihydro-5H-3,4-(azenometheno)[1,5]oxazocino[4,3,2-de]quinolin-6-ol or a salt thereof; optionally substituted (S)-2-amino-12-(ethoxymethyl)-6,7-dihydro-5H-3,4-(azenometheno)[1,5]oxazocino-[4,3,2-de]quinolin-6-ol or a salt thereof; optionally substituted 2-amino-12-(ethoxymethyl)-5H-3,4-(azenometheno)[1,5]oxazocino[4,3,2-de]quinolin-6(7H)-one or a salt thereof; or optionally substituted tert-butyl 4-((4-amino-2-(ethoxymethyl)-1-methyl-1H-imidazo[4,5-c]quinolin-9-yl)oxy)piperidine-1-carboxylate or a salt thereof.

TABLE 3 Compound Name Structure 9-methoxy-1H-imidazo[4,5-c]quinolin-4-amine

1-(4-amino-2-(ethoxymethyl)-9-methoxy-1H- imidazo[4,5-c]quinolin-1-yl)-2-methylpropan-2-ol

2-(ethoxymethyl)-1-isobutyl-9-methoxy-1H- imidazo[4,5-c]quinolin-4-amine

1-(4-amino-9-methoxy-2-(2-methoxyethyl)-1H- imidazo[4,5-c]quinolin-1-yl)-2-methylpropan-2-ol

1-(4-amino-2-(2-hydroxyethyl)-9-methoxy-1H- imidazo[4,5-c]quinolin-1-yl)-2-methylpropan-2-ol

4-((4-amino-2-(ethoxymethyl)-1H-imidazo[4,5- c]quinolin-9-yl)oxy)-2-methylbutan-2-ol

2-(ethoxymethyl)-9-(isopentyloxy)-1H- imidazo[4,5-c]quinolin-4-amine

4-((4-amino-2-(ethoxymethyl)-1H-imidazo[4,5- c]quinolin-9-yl)oxy)butan-2-ol

1-((4-amino-2-(ethoxymethyl)-1H-imidazo[4,5- c]quinolin-9-yl)oxy)propan-2-ol

4-((4-amino-2-(2-methoxyethyl)-1H-imidazo[4,5- c]quinolin-9-yl)oxy)-2-methylbutan-2-ol

4-((4-amino-2-(ethoxymethyl)-1-methyl-1H- imidazo[4,5-c]quinolin-9-yl)oxy)-2-methylbutan- 2-ol

2-(ethoxymethyl)-9-(2-isopropoxyethoxy)- 1H-imidazo[4,5-c]quinolin-4-amine

4-((4-amino-2-(ethoxymethyl)-1-isobutyl-1H- imidazo[4,5-c]quinolin-9-yl)oxy)-2-methylbutan- 2-ol

2-(ethoxymethyl)-1-(2-isopropoxyethyl)-9- methoxy-1H-imidazo[4,5-c]quinolin-4-amine

4-(4-amino-2-(ethoxymethyl)-9-methoxy-1H- imidazo[4,5-c]quinolin-1-yl)-2-methylbutan-2-ol

2-(ethoxymethyl)-9-isobutoxy-1H-imidazo[4,5- c]quinolin-4-amine

2-(ethoxymethyl)-9-(2-isopropoxyethoxy)-1- methyl-1H-imidazo[4,5-c]quinolin-4-amine

2-(ethoxymethyl)-9-isobutoxy-1-methyl-1H- imidazo[4,5-c]quinolin-4-amine

2-(ethoxymethyl)-9-isobutoxy-1-methyl-1H- imidazo[4,5-c]quinolin-4-amine

N-(3-((4-amino-2-(ethoxymethyl)-1-methyl-1H- imidazo[4,5-c]quinolin-9- yl)oxy)propyl)methanesulfonamide

N-(2-(2-((4-amino-2-(ethoxymethyl)-1-methyl- 1H-imidazo[4,5-c]quinolin-9- yl)oxy)ethoxy)ethyl)methanesulfonamide

N-(3-((4-amino-2-(ethoxymethyl)-1-methyl-1H- imidazo[4,5-c]quinolin-9- yl)oxy)propyl)acetamide

N-(4-((4-amino-2-(ethoxymethyl)-1-methyl-1H- imidazo[4,5-c]quinolin-9- yl)oxy)butyl)methanesulfonamide

N-(3-((4-amino-2-(ethoxymethyl)-1-methyl-1H- imidazo[4,5-c]quinolin-9- yl)oxy)propyl)stearamide

N-(4-((4-amino-2-(ethoxymethyl)-1-methyl-1H- imidazo[4,5-c]quinolin-9-yl)oxy)butyl)acetamide

N-(4-((4-amino-2-(ethoxymethyl)-1-methyl-1H- imidazo[4,5-c]quinolin-9-yl)oxy)butyl)stearamide

2-(ethoxymethyl)-1-methyl-9-(2- morpholinoethoxy)-1H-imidazo[4,5-c]quinolin-4- amine

2-(ethoxymethyl)-1-methyl-9-((tetrahydrofuran-3- yl)oxy)-1H-imidazo[4,5-c]quinolin-4-amine

2-(ethoxymethyl)-1-methyl-9-(pyrrolidin-3- yloxy)-1H-imidazo[4,5-c]quinolin-4-amine

2-(ethoxymethyl)-1-methyl-9-(piperidin-4-yloxy)- 1H-imidazo[4,5-c]quinolin-4-amine

N-(3-((4-amino-2-(ethoxymethyl)-1-methyl-1H- imidazo[4,5-c]quinolin-9- yl)oxy)propyl)palmitamide

N-(4-((4-amino-2-(ethoxymethyl)-1-methyl-1H- imidazo[4,5-c]quinolin-9- yl)oxy)butyl)palmitamide

9-(3-aminopropoxy)-2-(ethoxymethyl)-1-methyl- 1H-imidazo[4,5-c]quinolin-4-amine

2-(ethoxymethyl)-9-isopropoxy-1-methyl-1H- imidazo[4,5-c]quinolin-4-amine

1-((4-amino-2-(ethoxymethyl)-1-methyl-1H- imidazo[4,5-c]quinolin-9-yl)oxy)-2- methylpropan-2-ol

2-(ethoxymethyl)-3,4-dihydro-5-oxa-1,2a,9- triazanaphtho[2,1,8-cde]azulen-10-amine

(R)-2-(10-amino-2-(ethoxymethyl)-3,4-dihydro-5- oxa-1,2a,9-triazanaphtho[2,1,8-cde]azulen-3- yl)propan-2-ol

(S)-2-(10-amino-2-(ethoxymethyl)-3,4-dihydro-5- oxa-1,2a,9-triazanaphtho[2,1,8-cde]azulen-3- yl)propan-2-ol

(S)-2-amino-12-(ethoxymethyl)-6-methyl-6,7- dihydro-5H-3,4- (azenometheno)[1,5]oxazocino[4,3,2-de]quinolin- 6-ol

(R)-2-amino-12-(ethoxymethyl)-6-methyl-6,7- dihydro-5H-3,4- (azenometheno)[1,5]oxazocino[4,3,2-de]quinolin- 6-ol

(R)-2-amino-12-(ethoxymethyl)-6,7-dihydro-5H- 3,4-(azenometheno)[1,5]oxazocino[4,3,2- de]quinolin-6-ol

(S)-2-amino-12-(ethoxymethyl)-6,7-dihydro-5H- 3,4-(azenometheno)[1,5]oxazocino[4,3,2- de]quinolin-6-ol

2-amino-12-(ethoxymethyl)-5H-3,4- (azenometheno)[1,5]oxazocino[4,3,2-de]quinolin- 6(7H)-one

tert-butyl 4-((4-amino-2-(ethoxymethyl)-1- methyl-1H-imidazo[4,5-c]quinolin-9- yl)oxy)piperidine-1-carboxylate

Some embodiments include optionally substituted 4-amino-2H-pyrazolo[3,4-c]quinolin-9-ol or a salt thereof or optionally substituted 4-amino-2-isopentyl-2H-pyrazolo[3,4-c]quinolin-9-ol or a salt thereof optionally substituted 2-isopentyl-9-(isopentyloxy)-2H-pyrazolo[3,4-c]quinolin-4-amine or a salt thereof; or optionally substituted 2-butyl-9-(isopentyloxy)-2H-pyrazolo[3,4-c]quinolin-4-amine or a salt thereof.

TABLE 4 Compound Name Structure 4-amino-2H-pyrazolo[3,4-c]quinolin-9-ol

4-amino-2-isopentyl-2H-pyrazolo[3,4-c]quinolin- 9-ol

2-isopentyl-9-(isopentyloxy)-2H-pyrazolo[3,4- c]quinolin-4-amine

2-butyl-9-(isopentyloxy)-2H-pyrazolo[3,4- c]quinolin-4-amine

The following embodiments are specifically contemplated herein.

Embodiment 1. A compound represented by a formula:

or a salt thereof;

wherein a dashed line represents the presence or absence of a bond;

A¹ is CR¹, NR^(1A), or N;

A² is CR², NR^(2A), O, or S;

B¹ is CR⁵ or N;

B² is CR⁶ or N;

B³ is CR⁷ or N;

R¹ and R² are independently F, Cl, Br, I, NO₂, CN, R^(a), —OR^(a), —NR^(a)R^(b), —NHCOR^(a), —NHSO₂R^(a), —OCOR^(a), or —SO₂R^(a);

X is a bond, O, NR^(a), —CO—, —SO—, or —SO₂—, —CONR^(a), hydrocarbyl, and R³ is H or C₁₋₃₀ organyl; or X-R³ is F or Cl;

R^(1A), R^(2A), R⁴, R^(a), and R^(b)are independently H or C₁₋₃₀ organyl;

R⁵, R⁶, and R⁷ are independently F, Cl, Br, I, NO₂, CN, R^(a), —OR^(a), —NR^(a)R^(b), —NHCOR^(a), —NHSO₂R^(a), —OCOR^(a), —SO₂R^(a), or —X¹—(C_(m)H_(2m)O₀₋₁)—Z—(C_(n)H_(2n+1)), —(C_(m)H_(2m)O₀₋₁)—Z—(C_(n)H_(2n+1)), wherein R⁵ and R⁶ or R⁶ and R⁷ can be optionally linked to form a ring;

wherein X¹ is a bond, O, NR^(a), —CO—, —SO—, or —SO₂—;

Z is a bond, O, NHSO₂, or NHCO;

m is 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10; and

n is 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, or 23.

Embodiment 2. The compound of embodiment 1, further represented by a formula:

or a salt thereof, wherein R³ is C₁₋₃₀ organyl. In some embodiments, R³ is C₁₋₃ alkyl optionally substituted with 1 to 6 R^(8A) groups, wherein each R^(8A) group is independently OH, oxide, C₁₋₆ organyl, or —O—(C₁₋₆ organyl).

Embodiment 3. The compound of embodiment 1, further represented by a formula:

or a salt thereof; wherein R⁴ is H, C₁₋₃₀ non-aromatic organyl, or C₁₋₃₀ aromatic organyl containing an aromatic group that is not directly attached to the N atom.

Embodiment 4. The compound of embodiment 1, 2 or 3, wherein R¹ or R^(1A) is C₁₋₁₂ optionally substituted alkyl.

Embodiment 5. The compound of embodiment 4, wherein R¹ or R^(1A) is —C_(r)H_(2r+1)O, or an ester thereof, wherein r is 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10.

Embodiment 6. The compound of embodiment 5, wherein R¹ or R^(1A) is —C₃H₇O.

Embodiment 7. The compound of embodiment 6, wherein R¹ or R^(1A) is —CH₂OCH₂CH₃.

Embodiment 8. The compound of embodiment 1, 2, 3, 4, 5, 6, or 7, wherein R² or R^(2A) is H or CI₁₋₁₂ 12 optionally substituted alkyl.

Embodiment 9. The compound of embodiment 8, wherein R² or R^(2A) is C₁₋₆ alkyl, or —C_(y)H_(2y+1)O or an ester thereof, wherein y is 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10.

Embodiment 10. The compound of embodiment 9, wherein R² or R^(2A) is —C₄H₉O.

Embodiment 11. The compound of embodiment 10, wherein R² or R^(2A) is —CH₂—CH(CH₃)₂—OH.

Embodiment 12. The compound of embodiment 8, wherein R² or R^(2A) is H.

Embodiment 13. The compound of embodiment 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, or 12, wherein R³ is C₁₋₃₀ optionally substituted alkyl.

Embodiment 14. The compound of embodiment 13, wherein R³ is C₁₋₁₀ alkyl, or —C_(w)H_(2w+1)O or an ester thereof, wherein w is 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10.

Embodiment 15. The compound of embodiment 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, or 13, wherein R³ is —(C_(t)H_(2t)O₀₋₁)—Ht, wherein t is 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10, and Ht is optionally substituted C₃₋₆ heterocyclyl.

Embodiment 16. The compound of embodiment 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, or 13, wherein R³ is —(C_(u)H_(2u)O₀₋₁)—Z—(C_(v)H_(2v+1)), wherein Z is a bond, O, NHSO₂, or NHCO, u is 0, 1, 2, 3, 4, 5, or 6, and v is 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, or 23.

Embodiment 17. The compound of embodiment 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, or 13, wherein R³ is —(C_(u)H_(2u)O₀₋₁)—NR^(a)R^(b), and u is 1, 2, 3, 4, 5, or 6, wherein R^(a) and R^(b) are independently H or C₁₋₆ alkyl.

Embodiment 18. The compound of embodiment 14, wherein R³ is C₅H₁₁O.

Embodiment 19. The compound of embodiment 18, wherein R³ is —CH₂—CH₂—CH(CH₃)₂OH.

Embodiment 20. The compound of embodiment 17, wherein R³ is —CH₂—CH₂—CH₂—NH₂.

Embodiment 21. The compound of embodiment 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, or 20, wherein R⁴ is H or C₁₋₆ alkyl.

Embodiment 22. The compound of embodiment 21, wherein R⁴ is H.

Embodiment 23. The compound of embodiment 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, or 22, wherein R⁵ is R^(a), F, Cl, —CO₂R^(a), —CONR^(a)R^(b), CN, —OR^(a), —NR^(a)R^(b), —OCOR^(a), or —SO₂R^(a), wherein R^(a) and R^(b) are independently H or C₁₋₆ alkyl.

Embodiment 24. The compound of embodiment 23, wherein R⁵ is H.

Embodiment 25. The compound of embodiment 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, or 22, wherein R⁵ is —(C_(m)H_(2m)O₀₋₁)—Z—(C_(n)H_(2n+1)), wherein Z is a bond, O, NHSO₂, or NHCO, m is 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10, and n is 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24 or 25.

Embodiment 26. The compound of embodiment 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, or 25, wherein R⁶ is R^(a), F, Cl, —CO₂R^(a), —CONR^(a)R^(b), CN, —OR^(a), —NR^(a)R^(b), —OCOR^(a), or —SO₂R^(a), wherein R^(a) and R^(b) are independently H or C₁₋₆ alkyl.

Embodiment 27. The compound of embodiment 26, wherein R⁶ is H.

Embodiment 28. The compound of embodiment 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24 or 25, wherein R⁶ is —(C_(m)H_(2m)O₀₋₁)—Z—(C_(n)H_(2n+1)), wherein Z is a bond, O, NHSO₂, or NHCO, m is 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10, and n is 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, or 23.

Embodiment 29. The compound of embodiment 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27 or 28, wherein R⁷ is Ra, F, Cl, —CO₂R^(a), —CONR^(a)R^(b), CN, —OR^(a), —NR^(a)R^(b), —OCOR^(a), or —SO₂R^(a), wherein R^(a) and R^(b) are independently H or C₁₋₆ alkyl.

Embodiment 30. The compound of embodiment 29, wherein R⁷ is H.

Embodiment 31. The compound of embodiment 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16,

17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, or 28, wherein R⁷ is —(C_(m)H_(2m)O₀₋₁)—Z—(C_(n)H_(2n+1)), wherein Z is a bond, O, NHSO₂, or NHCO, m is 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10, and n is 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, or 23.

Embodiment 32. The compound of embodiment 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, or 31, R⁸ is H, OH, or CH₃.

Embodiment 33. The compound of embodiment 32, wherein R⁸ is OH.

Embodiment 34. The compound of embodiment 32, wherein R⁸ is H.

Embodiment 35. A compound, which is:

a salt of any of these compounds, or an ester of any of these compounds having an —OH group.

Embodiment 36. A compound which is optionally substituted 9-methoxy-1H-imidazo[4,5-c]quinolin-4-amine.

Embodiment 37. A compound which is optionally substituted 9-methoxy-2H-pyrazolo[3,4-c]quinolin-4-amine.

Embodiment 38. The compound of embodiment 36, which is optionally substituted 1-(4-amino-2-(ethoxymethyl)-9-methoxy-1H-imidazo[4,5-c]quinolin-1-yl)-2- methylpropan-2-ol or a salt thereof; optionally substituted 2-(ethoxymethyl)-1-isobutyl-9-methoxy-1H-imidazo[4,5-c]quinolin-4-amine or a salt thereof; optionally substituted 1-(4-amino-9-methoxy-2-(2-methoxyethyl)-1H-imidazo[4,5-c]quinolin-1-yl)-2-methylpropan-2-ol or a salt thereof; optionally substituted 1-(4-amino-2-(2-hydroxyethyl)-9-methoxy-1H-imidazo[4,5-c]quinolin-1-yl)-2-methylpropan-2-ol or a salt thereof; optionally substituted 4-((4-amino-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-9-yl)oxy)-2-methylbutan-2-ol or a salt thereof; optionally substituted 2-(ethoxymethyl)-9-(isopentyloxy)-1H-imidazo[4,5-c]quinolin-4-amine or a salt thereof; optionally substituted 4-((4-amino-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-9-yl)oxy)butan-2-ol or a salt thereof; optionally substituted 1-((4-amino-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-9-yl)oxy)propan-2-ol or a salt thereof; optionally substituted 4-((4-amino-2-(2-methoxyethyl)-1H-imidazo[4,5-c]quinolin-9-yl)oxy)-2-methylbutan-2-ol or a salt thereof; optionally substituted 4-((4-amino-2-(ethoxymethyl)-1-methyl-1H-imidazo[4,5-c]quinolin-9-yl)oxy)-2-methylbutan-2-ol or a salt thereof; optionally substituted 2-(ethoxymethyl)-9-(2-isopropoxyethoxy)-1H-imidazo[4,5-c]quinolin-4-amine or a salt thereof; optionally substituted 4-((4-amino-2-(ethoxymethyl)-1-isobutyl-1H- imidazo[4,5-c]quinolin-9-yl)oxy)-2-methylbutan-2-ol or a salt thereof; optionally substituted 2-(ethoxymethyl)-1-(2-isopropoxyethyl)-9-methoxy-1H-imidazo[4,5-c]quinolin-4-amine or a salt thereof; optinoally substituted 4-(4-amino-2-(ethoxymethyl)-9-methoxy-1H-imidazo[4,5-c]quinolin-1-yl)-2-methylbutan-2-ol or a salt thereof; optionally substituted 2-(ethoxymethyl)-9-isobutoxy-1H-imidazo[4,5-c]quinolin-4-amine or a salt thereof; optionally substituted 2-(ethoxymethyl)-9-(2-isopropoxyethoxy)-1-methyl-1H-imidazo[4,5-c]quinolin-4-amine or a salt thereof; optionally substituted 2-(ethoxymethyl)-9-(isopentyloxy)-1-methyl-1H-imidazo[4,5-c]quinolin-4-amine or a salt thereof; optionally substituted 2-(ethoxymethyl)-9-isobutoxy-1-methyl-1H-imidazo[4,5-c]quinolin-4-amine or a salt thereof; optionally substituted N-(3-((4-amino-2-(ethoxymethyl)-1-methyl-1H-imidazo[4,5-c]quinolin-9-yl)oxy)propyl)methanesulfonamide or a salt thereof; optionally substituted N-(2-(2-((4-amino-2-(ethoxymethyl)-1-methyl-1H-imidazo[4,5-c]quinolin-9-yl)oxy)ethoxy)ethyl)-methanesulfonamide or a salt thereof; optionally substituted N-(3-((4-amino-2-(ethoxymethyl)-1-methyl-1H-imidazo[4,5-c]quinolin-9-yl)oxy)propyl)acetamide or a salt thereof; optionally substituted N-(4-((4-amino-2-(ethoxymethyl)-1-methyl-1H-imidazo[4,5-c]quinolin-9-yl)oxy)butyl)methane-sulfonamide or a salt thereof; optionally substituted N-(3-((4-amino-2-(ethoxymethyl)-1-methyl-1H-imidazo[4,5-c]quinolin-9-yl)oxy)propyl)stearamide or a salt thereof; optionally substituted N-(4-((4-amino-2-(ethoxymethyl)-1-methyl-1H-imidazo[4,5-c]quinolin-9-yl)oxy)butyl)acetamide or a salt thereof; optionally substituted N-(4-((4-amino-2-(ethoxymethyl)-1-methyl-1H-imidazo[4,5-c]quinolin-9-yl)oxy)butyl)-stearamide or a salt thereof; optionally substituted 2-(ethoxymethyl)-1-methyl-9-(2-morpholinoethoxy)-1H-imidazo[4,5-c]quinolin-4-amine or a salt thereof; optionally substituted 2-(ethoxymethyl)-1-methyl-9-((tetrahydrofuran-3-yl)oxy)-1H-imidazo[4,5-c]quinolin-4-amine or a salt thereof; optionally substituted 2-(ethoxymethyl)-1-methyl-9-(pyrrolidin-3-yloxy)-1H-imidazo[4,5-c]quinolin-4-amine or a salt thereof; optionally substituted 2-(ethoxymethyl)-1-methyl-9-(piperidin-4-yloxy)-1H-imidazo[4,5-c]quinolin-4-amine or a salt thereof; optionally substituted N-(3-((4-amino-2-(ethoxymethyl)-1-methyl-1H-imidazo[4,5-c]quinolin-9-yl)oxy)propyl)palmitamide or a salt thereof; optionally substituted N-(4-((4-amino-2-(ethoxymethyl)-1-methyl-1H-imidazo[4,5-c]quinolin-9-yl)oxy)butyl)palmitamide or a salt thereof; optionally substituted 9-(3-aminopropoxy)-2-(ethoxymethyl)-1-methyl-1H-imidazo[4,5-c]quinolin-4-amine or a salt thereof; optionally substituted 2-(ethoxymethyl)-9-isopropoxy-1-methyl-1H-imidazo[4,5-c]quinolin-4-amine or a salt thereof; optionally substituted 1-((4-amino-2-(ethoxymethyl)-1-methyl-1H-imidazo [4,5-c]quinolin-9-yl)oxy)-2-methylpropan-2-ol or a salt thereof; optionally substituted 2-(ethoxymethyl)-3,4-dihydro-5-oxa-1,2a,9-triazanaphtho[2,1,8-cde]azulen-10-amine or a salt thereof; optionally substituted (R)-2-(10-amino-2-(ethoxymethyl)-3,4-dihydro-5-oxa-1,2a,9-triazanaphtho[2,1,8-cde]azulen-3-yl)propan-2-ol or a salt thereof; optionally substituted (S)-2-(10-amino-2-(ethoxymethyl)-3,4-dihydro-5-oxa-1,2a,9-triazanaphtho[2,1,8-cde]azulen-3-yl)propan-2-ol or a salt thereof; optionally substituted (S)-2-amino-12-(ethoxymethyl)-6-methyl-6,7-dihydro-5H-3,4-(azenometheno)[1,5]oxazocino[4,3,2-de]quinolin-6-ol or a salt thereof; optionally substituted (R)-2-amino-12-(ethoxymethyl)-6-methyl-6,7-dihydro-5H-3,4-(azenometheno)[1,5]oxazocino[4,3,2-de]quinolin-6-ol or a salt thereof; optionally substituted (R)-2-amino-12-(ethoxymethyl)-6,7-dihydro-5H-3,4-(azenometheno)[1,5]oxazocino[4,3,2-de]quinolin-6-ol or a salt thereof; optionally substituted (S)-2-amino-12-(ethoxymethyl)-6,7-dihydro-5H-3,4-(azenometheno)[1,5]oxazocino-[4,3,2-de]quinolin-6-ol or a salt thereof; optionally substituted 2-amino-12-(ethoxymethyl)-5H-3,4-(azenometheno)[1,5]oxazocino[4,3,2-de]quinolin-6(7H)-one or a salt thereof; or optionally substituted tert-butyl 4-((4-amino-2-(ethoxymethyl)-1-methyl-1H-imidazo[4,5-c]quinolin-9-yl)oxy)piperidine-1-carboxylate or a salt thereof.

Embodiment 39. The compound of embodiment 37 which is optionally substituted 4-amino-2H-pyrazolo[3,4-c]quinolin-9-ol or a salt thereof; optionally substituted 4-amino-2-isopentyl-2H-pyrazolo[3,4-c]quinolin-9-ol or a salt thereof; optionally substituted 2-isopentyl-9-(isopentyloxy)-2H-pyrazolo[3,4-c]quinolin-4-amine or a salt thereof; or optionally substituted 2-butyl-9-(isopentyloxy)-2H-pyrazolo[3,4-c]quinolin-4-amine or a salt thereof.

Embodiment 40. A method of treating viral infection, cancer, or an allergic disease, comprising administering a compound according to embodiment 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36 37, 38, or 39, to a mammal in need thereof

Embodiment 41. Use of a compound of embodiment 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, or 39, in the manufacture of a medicament for the treatment of viral infection, cancer, or an allergic disease.

Embodiment 42. The method of embodiment 40 or use of embodiment 41, wherein the viral infection comprises HCV infection.

Embodiment 43. A dosage form suitable for administration to a mammal, comprising a compound of embodiment 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, or 39.

EXAMPLES

In the synthetic schemes described below, unless otherwise indicated all temperatures are set forth in degrees Celsius and all parts and percentages are by weight. Reagents and solvents were purchased from commercial suppliers such as Aldrich Chemical Company and were used without further purification unless otherwise indicated. Tetrahydrofuran (THF) and N,N-dimethylforamide (DMF) were purchased from commercial sources in Sure Seal bottles and used as received.

The reactions set forth below were done generally under a positive pressure of argon or nitrogen at an ambient temperature (unless otherwise stated) in anhydrous solvents. Glassware was oven dried and/or heat dried. The reactions were assayed by TLC and/or analyzed by LC-MS and terminated as judged by the consumption of starting material. Analytical thin layer chromatography (TLC) was performed on glass plates pre-coated with silica gel 60 F254 0.25 mm plates (EM Science), and visualized with UV light (254 nm) and/or heating with commercial ethanolic phosphomolybdic acid. Preparative thin layer chromatography (TLC) was performed on glass-plates pre-coated with silica gel 60 F254 0.5 mm plates (20×20 cm, from commercial sources) and visualized with UV light (254 nm).

Work-ups were typically done by doubling the reaction volume with the reaction solvent or extraction solvent and then washing with the indicated aqueous solutions using 25% by volume of the extraction volume unless otherwise indicated. Product solutions were dried over anhydrous Na₂SO₄ and/or Mg₂SO₄ prior to filtration and evaporation of the solvents under reduced pressure on a rotary evaporator and noted as solvents removed in vacuo. Column chromatography was completed under positive pressure using 230-400 mesh silica gel.

¹H-NMR spectra and ¹³C-NMR were recorded on a Varian Mercury-VX400 instrument operating at 400 MHZ. NMR spectra were obtained as CDCl₃ solutions (reported in ppm), using chloroform as the reference standard (7.27 ppm for the proton and 77.00 ppm for carbon), CD₃OD (3.4 and 4.8 ppm for the protons and 49.3 ppm for carbon), DMSO-d₆ (2.49 ppm for proton), or internally tetramethylsilane (0.00 ppm) when appropriate. Other NMR solvents were used as needed.

Example 1

Synthesis of 1-1[4-Amino-2-(ethoxymethyl)-9-methoxy-imidazo[4,5-c]quinolin-1-yl]-2-methyl-propan-2-ol

Step 1: Synthesis of 1-[(5-Methoxy-3-nitro-4-quinolyl)amino]-2-methyl-propan-2-ol

To a solution of 1-amino-2-methyl-propan-2-ol (747.10 mg, 8.38 mmol, 2.0 eq.) and Et₃N (2.12 g, 20.95 mmol, 2.90 mL, 5.0 eq.) in DCM (50.00 mL) was added 4-chloro-5-methoxy-3-nitro-quinoline (1.00 g, 4.19 mmol, 1.0 eq.). The resulting mixture was stirred at 25° C. for 0.5 h. The reaction mixture was washed with water (30 mL) and brine (30 mL) via extraction. The organic phase was dried over anhydrous Na₂SO₄, filtered, and concentrated in vacuo. The residue was purified with column chromatography (DCM to DCM/MeOH=20/1). The desired product of 1-[(5-methoxy-3-nitro-4-quinolyl)amino]-2-methyl-propan-2-ol (1.00 g, 3.43 mmol, 81.86% yield) was obtained as a yellow solid. ¹H NMR (400 MHz, CDCl₃) δ ppm: 9.51; (s, 1H), 9.03; (s, 1H), 7.63; (t, J=8.0 Hz, 1H), 7.58; (d, J=8.4 Hz, 1H), 6.94; (d, J=7.2 Hz, 1H), 4.10; (s, 3H), 2.95; (d, J=4.8 Hz, 2H), 1.29; (s, 6H); ES-LCMS m/z 292.3 [M+H]⁺.

Step 2: Synthesis of 1-[(3-Amino-5-methoxy-4-quinolyl)amino]-2-methyl-propan-2-ol

To a solution of 1-[(5-methoxy-3-nitro-4-quinolyl)amino]-2-methyl-propan-2-ol (1.00 g, 3.43 mmol, 1.0 eq.) in MeOH (100.00 mL) was added Raney-Ni (626.42 mg, 7.31 mmol, 2.1 eq.) under N2. The suspension was degassed under vacuum and purged with H₂ several times. The resulting mixture was stirred under H₂ (15 psi) at 25° C. for 3 h. The reaction mixture was filtered. The filtrate was concentrated in vacuo. The desired product of 1-[(3-amino-5-methoxy-4-quinolyl)amino]-2-methyl-propan-2-ol (870.00 mg, 3.33 mmol, 97.08% yield) was obtained as a yellow solid. ¹H NMR (400 MHz, CD₃OD) δ ppm: 8.26; (s, 1H), 7.38; (d, J=8.0 Hz, 1H), 7.31; (t, J=8.0 Hz, 1H), 6.88; (d, J=7.6 Hz, 1H), 4.02; (s, 3H), 3.22; (s, 2H), 1.29; (s, 6H); ES-LCMS m/z 262.3 [M+H]⁺.

Step 3: Synthesis of 1-[2-(Ethoxymethyl)-9-methoxy-imidazo[4,5-c]quinolin-1-yl]-2-methyl-propan-2-ol

A solution of 1-[(3-amino-5-methoxy-4-quinolyl)amino]-2-methyl-propan-2-ol (400.00 mg, 1.53 mmol, 1.0 eq.) and 4A MS (200 mg) in 2-ethoxyacetic acid (3.30 g, 31.7 mmol, 3 mL, 20.7 eq.) was stirred at 120° C. for 4 h under microwave. The reaction mixture was then filtered. The filtrate was dissolved in DCM (80 mL) and adjusted to pH=8 with 2 M NaOH. The organic layer was separated and dried over anhydrous Na2SO4, filtered and concentrated in vacuo. The mixture was purified with column chromatography (DCM to DCM/MeOH=10/1). The desired product of 1-2-(ethoxymethyl)-9-methoxy-imidazo[4,5-c]quinolin-1-yl1-2-methyl- propan-2-ol (230.00 mg, 698.26 mol, 45.62% yield) was obtained as a yellow solid. ¹H NMR (400 MHz, CD₃OD) δ ppm: 9.09; (s, 1H), 7.79; (d, J=8.0 Hz, 1H), 7.67; (t, J=8.2 Hz, 1H), 7.25; (d, J=7.2 Hz, 1H), 5.68; (s, 1H), 5.39; (s, 1H), 4.63; (m, 2H), 4.14; (s, 3H), 3.62; (m, 2H), 1.32-1.26; (m, 3H), 1.25-1.23; (m, 3H), 0.76; (m, 3H); ES-LCMS m/z: 330.3 [M+H]⁺.

Step 4: Synthesis of 1-[2-(Ethoxymethyl)-9-methoxy-5-oxido-imidazo[4,5-c]quinolin-5-ium-1-yl]2-methyl-propan-2-ol

To a solution of 1-[2-(ethoxymethyl)-9-methoxy-imidazo[4,5-c]quinolin-1-yl]-2-methyl-propan-2-ol (230.00 mg, 698.26 mol, 1.0 eq.) in DCM (30.00 mL) was added m-CPBA (212.64 mg, 1.05 mmol, 85% purity, 1.5 eq.). The resulting mixture was stirred at 25° C. for 1 h. The reaction mixture was then adjusted to pH=8 with aqueous K₂CO₃ and partitioned between DCM (50 mL) and water (20 mL). The organic layer was separated, washed with brine (20 mL), dried over Na₂SO₄, and filtered. After filtration, the filtrate was concentrated in vacuo. The residue was purified with prep-TLC (DCM/MeOH=8/1, R_(f)=0.3). The desired product of 1-[2-(ethoxymethyl)-9-methoxy-5-oxido-imidazo[4,5-c]quinolin-5-ium-1-yl]-2-methyl-propan-2-ol (150.00 mg, 434.29 μmol, 62.20% yield) was obtained as a yellow solid. ¹H NMR (400 MHz, CD₃OD) δ ppm: 9.10; (s, 1H), 8.52; (d, J=8.8 Hz, 1H), 7.85; (t, J=8.6 Hz, 1H), 7.45; (d, J=7.6 Hz, 1H), 5.54; (s, 1H), 5.31; (s, 1H), 4.58; (s, 2H), 4.19; (s, 3H), 3.62; (m, 2H), 1.28-1.23; (m, 6H), 0.84; (m, 3H); ES-LCMS m/z: 346.3 [M+H]⁺.

Step 5: Synthesis of 1-[4-Amino-2-(ethoxymethyl)-9-methoxy-imidazo[4,5-c]quinolin-1-yl]-2-methyl-propan-2-ol

To a solution of 1-[2-(ethoxymethyl)-9-methoxy-5-oxido-imidazo[4,5-c]quinolin-5-ium-1-yl]-2-methyl-propan-2-ol (150.00 mg, 434.29 mol, 1.0 eq.) and NH₃.H₂O (543.64 mg, 4.34 mmol, 597.41 μL, 28% purity, 10.0 eq.) in CHCl₃ (20.00 mL) was added TsCl (99.36 mg, 521.15 mol, 1.2 eq.). The resulting mixture was stirred at 20° C. for 0.5 h. The solvent was removed in vacuo. The residue was purified with prep-HPLC (MeCN/H₂O as eluents, acidic condition). After lyophilization, the desired product of 1-[4-amino-2-(ethoxymethyl)-9-methoxy-imidazo[4,5-c]quinolin-1-yl]-2-methyl-propan-2-ol (50.00 mg, 131.28 mol, 30.23% yield, 100% purity, as HCl salt) was obtained as a white solid. ¹H NMR (400 MHz, CD₃OD) δ ppm: 7.63; (t, J=8.2 Hz, 1H), 7.30; (d, J=8.0 Hz, 1H), 7.13; (d, J=8.0 Hz, 1H), 5.50; (s, 1H), 5.21; (s, 1H), 4.76; (s, 1H), 4.55; (s, 1H), 4.09; (s, 3H), 3.59; (m, 2H), 1.23-1.20; (m, 6H), 0.82; (m, 3H); ES-LCMS m/z: 345.3 [M+H]⁺

Example 2

Synthesis of 2-(Ethoxymethyl)-1-isobutyl-9-methoxy-imidazo[4,5-c]quinolin-4-amine

Step 1: Synthesis of 2-(Ethoxymethyl)-1-isobutyl-9-methoxy-imidazo[4,5-c]quinoline

To a solution of N⁴-isobutyl-5-methoxy-quinoline-3,4-diamine (100.00 mg, 407.63 μmol, 1.0 eq.) and pyridine (322.44 mg, 4.08 mmol, 329.02 μL, 10.0 eq.) in DCM (4.00 mL) was added 2-ethoxyacetyl chloride (99.91 mg, 815.26 μmol, 2.0 eq.). The resulting mixture was stirred at 25° C. for 1 h. The solvent was removed in vacuo. The residue was dissolved in NaOH (2 M, 4.95 mL, 24.3 eq.) and stirred at 100° C. for 5 h. The mixture was dissolved in water (10 mL) and extracted with DCM (50 mL×2). The combined organic phase was washed with brine (20 mL), dried over anhydrous Na₂SO₄, filtered and concentrated in vacuo. The residue was purified with prep-TLC (DCM/MeOH=15/1). The desired product of 2-(ethoxymethyl)-1-isobutyl-9-methoxy-imidazo[4,5-c]quinoline (80.00 mg, 255.27 μmol, 62.62% yield) was obtained as a brown solid. ¹H NMR (400 MHz, CDCl₃) δ ppm: 9.27; (s, 1H), 7.70; (d, J=8.4 Hz, 1H), 7.60; (t, J=8.2 Hz, 1H), 7.04; (d, J=8.0 Hz, 1H), 4.89; (s, 2H), 4.62; (br, s. 2H), 4.08; (s, 3H), 3.65-3.59; (m, 2H), 2.11-2.02; (m, 1H), 1.26; (t, J=7.0 Hz, 3H), 0.75-0.72; (m, 6H); ES-LCMS m/z: 314.3 [M+H]⁺.

Step 2: 2-(Ethoxymethyl)-1-isobutyl-9-methoxy-5-oxido-imidazo[4,5-c]quinolin-5-ium

To a solution of 2-(ethoxymethyl)-1-isobutyl-9-methoxy-imidazo[4,5-c]quinoline (50.00 mg, 159.55 μmol , 1.0 eq.) in DCM (5.00 mL) was added m-CPBA (48.59 mg, 239.33 μmol, 85% purity, 1.5 eq.). The resulting mixture was stirred at 25° C. for 0.5 h. DCM (40 mL) and water (10 mL) were added, and pH was adjusted to 8 by addition of aqueous NaOH. The organic layer was then separated, washed with brine (10 mL), dried over Na₂SO₄ and filtered. The filtrate was concentrated in vacuo. The desired product of 2-(ethoxymethyl)-1-isobutyl-9-methoxy-5-oxido-imidazo[4,5-c]quinolin-5-ium (50.00 mg, 151.80 mol, 95.14% yield) was obtained as a yellow solid. ¹H NMR (400 MHz, CDCl₃) δ ppm: 9.05; (s, 1H), 8.71; (d, J=8.8 Hz, 1H), 7.70; (t, J=8.2 Hz, 1H), 7.17; (d, J=7.2 Hz, 1H), 4.56; (s, 2H), 4.44; (br, s. 2H), 4.11; (s, 3H), 3.65-3.59; (m, 2H), 2.06-1.99; (m, 1H), 1.27; (t, J=7.0 Hz, 3H), 0.76-0.72; (m, 6H); ES-LCMS m/z: 330.2 [M+H]⁺.

Step 3: 2-(Ethoxymethyl)-1-isobutyl-9-methoxy-imidazo[4,5-e]quinolin-4-amine

To a solution of 2-(ethoxymethyl)-1-isobutyl-9-methoxy-5-oxido-imidazo[4,5-c]-quinolin-5-ium (50.00 mg, 151.80 μmol, 1.0 eq.) and NH₃.H₂O (190.27 mg, 1.52 mmol, 209.09 μL, 28% purity, 10.0 eq.) in CHCl₃ (10.00 mL) was added TsCl (34.73 mg, 182.16 mol, 1.2 eq.). The resulting mixture was stirred at 25° C. for 0.5 h. The solvent was removed in vacuo. The residue was purified with prep-HPLC (MeCN/H₂O as eluents, acidic condition). After lyophilization, the desired product of 2-(ethoxymethyl)-1-isobutyl-9-methoxy-imidazo[4,5-c]quinolin-4-amine (30.00 mg, 78.31 mol, 51.59% yield, 95.24% purity, as HCl salt) was obtained as a white solid. ¹H NMR (400 MHz, CD₃OD) δ ppm: 7.69; (t, J=8.2 Hz, 1H), 7.36; (d, J=8.0 Hz, 1H), 7.18; (d, J=8.4 Hz, 1H), 4.87; (s, 2H), 4.62; (br, s. 2H), 4.13; (s, 3H), 3.69-3.64; (m, 2H), 2.05-1.95; (m, 1H), 1.27; (t, J=7.0 Hz, 3H), 0.80-0.75; (m, 6H); ES-LCMS m/z: 329.4 [M+H]⁺.

The following compounds were prepared using the same method as that in Example 1 or 2 using corresponding reagents.

1-[4-Amino-9-methoxy-2-(2-methoxyethyl)imidazo[4,5-c]quinolin-1-yl]-2-methyl-propan-2-ol was obtained as a white solid in 9.18% yield as a HCl salt with 98.5% purity. ¹H NMR (400 MHz, CD₃OD) δ ppm: 7.67; (t, J=8.4 Hz, 1H), 7.35; (d, J=8.4 Hz, 1H), 7.18; (d, J=8.4 Hz, 1H), 5.60; (m, 1H), 4.48; (m, 1H), 4.14; (s, 3H), 3.97; (m, 2H), 3.47-3.44 (m, 2H), 3.42; (s, 3H), 1.26; (s, 3H), 0.89; (s, 3H); ES-LCMS m/z: 345.3 [M+H]⁺.

1-[4-Amino-2-(2-hydroxyethyl)-9-methoxy-imidazo [4,5 -c] quinolin-1-yl]-2-methyl-pro-pan-2-ol was obtained as a white solid in 3.47% yield as a HCl salt with100% purity. ¹H NMR (400 MHz, CD₃OD) δ ppm: 7.61; (t, J=8.4 Hz, 1H), 7.28; (d, J=8.0 Hz, 1H), 7.12; (d, J=7.6 Hz, 1H), 5.54; (m, 1H), 4.41; (m, 1H), 4.08; (s, 3H), 4.07-4.05; (m, 2H), 3.27; (m, 2H), 1.20; (s, 3H), 0.85; (s, 3H); ES-LCMS m/z: 331.2 [M+H].

4-[[4-Amino-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-9-yl]oxy]-2-methyl-butan-2-ol was obtained as a white solid in 40.57% yield as a HCl salt. ¹H NMR (400 MHz, CD₃OD) δ ppm: 7.68; (t, J=8.4 Hz, 1H), 7.34; (d, J=8.4 Hz, 1H), 7.15; (d, J=8.4 Hz, 1H), 4.84; (s, 2H), 4.50; (t, J=6.0 Hz, 2H), 3.76-3.70; (m, 2H), 2.19; (t, J=5.8 Hz, 2H), 1.43; (s, 6H), 1.31; (t, J=7.0 Hz, 3H); ES-LCMS m/z: 345.3 [M+H]⁺.

Example 3

Synthesis of 2-(Ethoxymethyl)-9-isopentyloxy-1H-imidazo[4,5-c]quinolin-4-amine

Step 1: Synthesis of 5-Isopentyloxy-3-nitro-quinolin-4-amine

To a solution of 4-amino-3-nitro-quinolin-5-ol (300.00 mg, 1.46 mmol, 1.0 eq.), TBAB (470.66 mg, 1.46 mmol, 1.0 eq.) and KI (242.36 mg, 1.46 mmol, 1.0 eq.) in NaOH (1 M, 4.38 mL, 3.0 eq.) was added a solution of isopentyl 4-methylbenzenesulfonate (1.06 g, 4.38 mmol, 3.0 eq.) in DCM (4.00 mL). The resulting mixture was stirred at 20° C. for 40 h. The reaction mixture was diluted with H₂O (10 mL) and extracted with DCM (30 mL×2). The combined organic layers were washed with brine (10 mL), dried over Na2SO4, filtered and concentrated under reduced pressure to give a residue. The residue was purified with column chromatography (PE to PE/EA=1/2). The desired product of 5-isopentyloxy- 3-nitro-quinolin-4-amine (140.00 mg, 508.54 μmol, 34.83% yield) was obtained as a yellow solid. ¹H NMR (400 MHz, CDCl₃) δ ppm: 9.33; (s, 1H), 9.25; (s, 1H), 9.10; (s, 1H), 7.66; (t, J=8.2 Hz, 1H), 7.57; (d, J=8.4 Hz, 1H), 6.94; (d, J=7.6 Hz, 1H), 4.28; (t, J=6.2 Hz, 2H), 1.88; (m, 3H), 1.05; (d, J=6.0 Hz, 6H); ES-LCMS m/z: 276.3 [M+H]⁺.

Step 2: Synthesis of 5-Isopentyloxyquinoline-3,4-diamine

To a solution of 5-isopentyloxy-3-nitro-quinolin-4-amine (140.00 mg, 508.54 μmol , 1.0 eq.) in MeOH (50.00 mL) was added Raney-Ni (100.00 mg, 1.17 mmol, 2.3 eq.) under N₂. The suspension was degassed under vacuum and purged with H₂ three times. The resulting mixture was stirred under H₂ (15 psi) at 20° C. for 2 h. The reaction mixture was filtered. The filtrate was concentrated in vacuo. The desired product of 5-isopentyloxyquinoline-3,4-diamine (120.00 mg, 489.16 μmol, 96.19% yield) was obtained as a green solid. ¹H NMR (400 MHz, CD₃OD) δ ppm: 8.01; (s, 1H), 7.53; (t, J=8.2 Hz, 1H), 7.27; (d, J=8.8 Hz, 1H), 6.96; (d, J=8.0 Hz, 1H), 4.30; (t, J=6.2 Hz, 2H), 1.89-1.87; (m, 3H), 1.04; (d, J=6.4 Hz, 6H); ES-LCMS m/z: 246.3 [M+H]⁺.

Step 3: Synthesis of 2-(Ethoxymethyl)-9-isopentyloxy-1H-imidazo [4, 5-c]quinoline

5-Isopentyloxyquinoline-3,4-diamine (110.00 mg, 448.39 μmol, 1.0 eq.), 2-ethoxyacetic acid (1.21 g, 11.62 mmol, 1.10 mL, 25.9 eq.) and 4 Å MS (150.00 mg) were placed into a microwave tube. The sealed tube was heated at 130° C. for 1 h under microwave. The solid was filtered off. The filtrate was diluted with DCM (50 mL) and water (20 mL). The mixture was adjusted to pH=7 with aqueous NaOH (1 M). The layers were separated. The organic phase was washed with brine (20 mL), dried over anhydrous Na₂SO4, filtered and concentrated in vacuo. The residue was purified with prep-TLC (DCM/MeOH=20/1). The desired product of 2-(ethoxymethyl)-9-isopentyloxy-1H-imidazo[4,5-c]quinoline (130.00 mg, 414.82 μmol, 92.51% yield) was obtained as a yellow solid. ¹H NMR (400 MHz, CD₃OD) δ ppm: 9.10; (s, 1H), 7.73; (d, J=8.8 Hz, 1H), 7.66; (t, J=8.4 Hz, 1H), 7.20; (d, J=7.6 Hz, 1H), 4.80; (s, 2H), 4.48; (t, J=6.6 Hz, 2H), 3.73-3.68; (m, 2H), 1.95-1.88; (m, 3H), 1.29; (t, J=7.0 Hz, 3H), 1.05; (d, J=6.0 Hz, 6H); ES-LCMS m/z: 314.3 [M+H]⁺.

Step 4: Synthesis of 2-(Ethoxymethyl)-9-isopentyloxy-5-oxido-1H-imidazo [4,5-c]quinolin-5-ium

To a solution of 2-(ethoxymethyl)-9-isopentyloxy-1H-imidazo[4,5-c]quinoline (130.00 mg, 414.82 μmol , 1.0 eq.) in DCM (30.00 mL) was added m-CPBA (126.33 mg, 622.23 μmol, 85% purity, 1.5 eq.). The resulting mixture was stirred at 20° C. for 0.5 h. The reaction mixture was diluted with DCM (20 mL) and washed with saturated K₂CO₃ (10 mL) via extraction. The combined organic layers were washed with brine (15 mL), dried over Na₂SO₄, filtered and concentrated under reduced pressure. The desired product of 2-(ethoxymethyl)-9-isopentyloxy-5-oxido-1H-imidazo[4,5-c]quinolin-5-ium (130.00 mg, 394.67 mol, 95.14% yield) was obtained as a brown solid. ¹H NMR (400 MHz, CD₃OD) δ ppm: 9.11; (s, 1H), 8.31; (d, J=8.4 Hz, 1H), 7.82; (t, J=8.8 Hz, 1H), 7.41-7.38; (m, 1H), 4.88 (s, 2H), 4.54; (t, J=6.6 Hz, 2H), 3.73-3.67; (m, 2H), 1.94-1.86; (m, 3H), 1.29; (t, J=7.0 Hz, 3H), 1.04; (d, J=6.0 Hz, 6H); ES-LCMS m/z: 330.3 [M+H]⁺.

Step 5: Synthesis of 2-(Ethoxymethyl)-9-isopentyloxy-1H-imidazo[4,5-c]quinolin-4-amine

To a solution of 2-(ethoxymethyl)-9-isopentyloxy-5-oxido-1H-imidazo[4,5-c]-quinolin-5-ium (130.00 mg, 394.67 mol, 1.0 eq.) and NH₃.H₂O (494.04 mg, 3.95 mmol, 542.90 μL, 28% purity, 10.0 eq.) in CHCl₃ (6.00 mL) was added TsCl (112.87 mg, 592.00 μmol, 1.5 eq.). The resulting mixture was stirred at 25° C. for 0.5 h. The solvent was then removed in vacuo. The residue was purified with prep-HPLC (MeCN/H₂O as eluents, acidic condition). After lyophilization, the desired product of 2-(ethoxymethyl)-9-isopentyloxy-1H-imidazo[4,5-c]quinolin-4-amine (75.00 mg, 196.61 49.82% yield, 95.65% purity, as HCl salt) was obtained as a white solid. ¹H NMR (400 MHz, CD₃OD) δ ppm: 7.68; (t, J=8.2 Hz, 1H), 7.33; (d, J=8.4 Hz, 1H), 7.17; (d, J=8.4 Hz, 1H), 4.86; (s, 2H), 4.51; (t, J=6.8 Hz, 2H), 3.75-3.70; (m, 2H), 1.94-1.86; (m, 3H), 1.31; (t, J=7.0 Hz, 3H), 1.05; (d, J=6.4 Hz, 6H); ES-LCMS m/z: 329.3 [M+H]⁺.

The following compound was prepared using the same method as that described in Example 3 using corresponding reagents.

4-[[4-Amino-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-9-yl]oxy]butan-2-ol HCl salt was obtained in 20.06% yield with100% purity as a white solid. ¹H NMR (400MHz, CD₃OD) δ ppm: 7.65; (t, J=8.4 Hz, 1H), 7.31; (d, J=8.0 Hz, 1H), 7.13; (d, J=8.4 Hz, 1H), 4.79; (s, 2H), 4.54-4.53; (m, 1H), 4.42-4.40; (m, 1H), 4.25-4.16; (m, 1H), 3.72-3.66; (m, 2H), 2.15-2.09; (m, 2H), 1.35; (d, J=6.4 Hz, 3H), 1.27; (t, J=7.0 Hz, 3H); ES-LCMS m/z: 330.9 [M+H]⁺.

Example 4

Synthesis of 1-((4-amino-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-9-yl)oxy)propan-2-ol

Step 1: Synthesis of 1-[(4-Amino-3-nitro-5-quinolyl)oxy]propan-2-one

To a solution of 4-amino-3-nitro-quinolin-5-ol (1.00 g, 4.87 mmol, 1.0 eq.), TBAB (1.57 g, 4.87 mmol, 1.0 eq.), KI (809.09 mg, 4.87 mmol, 1.0 eq.) in NaOH (2 M, 7.31 mL, 3.0 eq.) was added acetonyl 4-methylbenzenesulfonate (3.33 g, 14.61 mmol, 3.0 eq.) in DCM (8.00 mL) at 25° C. The mixture was stirred at 25° C. for 48 h. The reaction mixture was diluted with H₂O (20 mL) and extracted with DCM (50 mL×2). The combined organic layers were washed with brine (20 mL), dried over Na₂SO₄, filtered and concentrated under reduced pressure to give a residue. The residue was purified with column chromatography (DCM to DCM/MeOH=20/1). The desired product of 1-[(4-amino-3-nitro-5-quinolyl)oxy]propan-2-one (220.00 mg, 842.17 μmol, 17.29% yield) was obtained as a yellow solid. ¹H NMR (400 MHz, CDCl₃) δ ppm: 9.84; (br s, 1H), 9.41; (br s, 1H), 9.35; (s, 1H), 7.66-7.60; (m, 2H), 6.80-6.77; (m, 1H), 4.92; (s, 2H), 2.37; (s, 3H); ES-LCMS m/z: 262.2 [M+H]⁺.

Step 2: Synthesis of 1-[(3,4-Diamino-5-quinolyl)oxy]propan-2-ol

To a solution of 1-[(4-amino-3-nitro-5-quinolyl)oxy]propan-2-one (220.00 mg, 842.17 μmol, 1.0 eq.) in MeOH (100.00 mL) was added Raney-Ni (100.29 mg, 1.17 mmol, 1.39 eq.) under N₂. The suspension was degassed under vacuum and purged with H₂ several times. The mixture was stirred under H2 (15 psi) at 25° C. for 1 h. The solid was filtered off The filtrate was concentrated in vacuo. The desired product of 1-[(3,4-diamino-5-quinoyl)oxy]-propan-2-ol (160.00 mg, 685.90 μmol, 81.44% yield) was obtained as a green solid. ¹H NMR (400 MHz, CD₃OD) δ ppm: 7.95; (s, 1H), 7.64-7.60; (m, 1H), 7.28-7.26 (m, 1H), 7.02-6.90; (m, 1H), 4.32-4.29; (m, 2H), 4.07-4.04; (m, 1H), 1.33 (d, J=6.4 Hz, 3H); ES-LCMS m/z: 234.1 [M+H]⁺.

Step 3: Synthesis of 1-[[2-(Ethoxymethyl)-1H-imidazo[4,5-c]quinolin-9-yl]oxy]propan-2-ol

1-[(3,4-Diamino-5-quinolyl)oxy]propan-2-ol (150.00 mg, 643.03 mol, 1.0 eq.), 2-ethoxyacetic acid (1.10 g, 10.57 mmol, 1.00 mL, 16.4 eq.) and 4 Å MS (50.00 mg) were placed into a microwave tube. The sealed tube was heated at 120° C. for 0.5 h under microwave. An aqueous solution of 3 M NaOH (10 mL) and THF (3 mL) were added into the reaction mixture. The resulting mixture was stirred at 50° C. for 2 h. The mixture was extracted with ethyl acetate (50 mL×3). The combined organic layers were washed with saturated brine (10 mL), dried over anhydrous Na₂SO₄, filtered and concentrated under reduced pressure to give a residue. The residue was purified with prep-TLC (DCM/MeOH=15/1). The desired product of 1-[[2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-9-yl]oxy]-propan-2-ol (23.00 mg, 76.33 μmol, 11.87% yield) was obtained as a yellow solid. ¹H NMR (400 MHz, CDCl₃) δ ppm: 11.52; (s, 1H), 9.20; (s, 1H), 7.81; (d, J=8.4 Hz, 1H), 7.50; (t, J=8.0 Hz, 1H), 6.97; (d, J=7.6 Hz, 1H), 4.83; (s, 2H), 4.42; (m, 1H), 4.32-4.28; (m, 1H), 4.02; (t, J=8.2 Hz, 1H), 3.64-3.61; (m, 2H), 1.40; (m, 3H), 1.25; (m, 3H); ES-LCMS m/z: 302.2 [M+H]⁺.

Step 4: Synthesis of 1-[[2-(Ethoxymethyl)-5-oxido-1H-imidazo[4,5-c]quinolin-5-ium-9-yl]oxy]propan-2-ol

To a mixture of 1-[[2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-9-yl]oxy]propan-2-ol (23.00 mg, 76.33 μmol, 1.0 eq.) in DCM (8.00 mL) was added m-CPBA (30.99 mg, 152.65 μmol, 85% purity, 2.0 eq.) in one portion at 25° C. The mixture was stirred at 25° C. for 1 h. The solvent was removed in vacuo. The crude product was used for the next step without further purification. The crude product of 1-[[2-(ethoxymethyl)-5-oxido-1H-imidazo[4,5-c]-quinolin-5-ium-9-yl]oxy]propan-2-ol (20.00 mg, 63.02 μmol, 82.57% yield) was obtained as a brown solid. ¹H NMR (400 MHz, CDCl₃) δ ppm: 9.17; (s, 1H), 8.39; (d, J=8.8 Hz, 1H), 7.47-7.45; (m, 1H), 7.05-7.01; (m, 1H), 4.86; (s, 2H), 4.48; (m, 1H), 4.37; (m, 1H), 4.06; (d, J=8.4 Hz, 1H), 3.74-3.71; (m, 2H), 1.47; (br d, J=6.4 Hz, 3H), 1.35; (t, J=7.2 Hz, 3H); ES-LCMS m/z:=318.2 [M+H]⁺.

Step 5: Synthesis of 1-[[4-Amino-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-9-yl]oxy]-propan-2-ol

To a mixture of 1-[[2-(ethoxymethyl)-5-oxido-1H-imidazo[4,5-c]quinolin-5-ium-9-yl]oxy]propan-2-ol (20.00 mg, 63.02 mol, 1.0 eq.) and NH₃.H₂O (78.89 mg, 630.24 μmol, 86.69 μL, 28% purity, 10.0 eq.) in CHCl₃ (6.00 mL) was added TsCl (24.03 mg, 126.05 μmol, 2.0 eq.) at 25° C. The mixture was stirred at 25° C. for 3 h. The reaction mixture was concentrated under reduced pressure to remove the solvent. The residue was purified with preparative HPLC (MeCN/H₂O as eluents, acidic condition). After lyophilization, the desired product of 1-[[4-amino-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-9-yl]oxy]propan-2-ol (4.68 mg, 13.26 mol, 21.04% yield, as HCl salt) was obtained as a white solid. ¹H NMR (400 MHz, CD₃OD) δ ppm: 7.66; (t, J=8.4 Hz, 1H), 7.35; (d, J=8.4 Hz, 1H), 7.20; (d, J=8.4 Hz, 1H), 4.83; (s, 2H), 4.42-4.39; (m, 1H), 4.36; (m, 1H), 4.18-4.16; (m, 1H), 3.71-3.68; (m, 2H), 1.36; (d, J=6.4 Hz, 3H), 1.29; (t, J=7.2 Hz, 3H); ES-LCMS m/z: 317.2 [M+H]⁺.

Example 5

Synthesis of 4-[[4-Amino-2-(2-methoxyethyl)-1H-imidazo[4,5-c]quinolin-9-yl]oxy]-2-methyl-butan-2-ol

Step 1: Synthesis of 4-[[2-(2-Methoxyethyl)-1H-imidazo[4,5-c]quinolin-9-yl]oxy]-2-methyl-butan-2-ol

To a solution of 4-[(3,4-diamino-5-quinolyl)oxy]-2-methyl-butan-2-ol (179.17 mg, 329.10 mol, 1.0 eq.) and pyridine (260.32 mg, 3.29 mmol, 265.63 μL, 10.0 eq.) in DCM (2.00 mL) was added 3-methoxypropanoyl chloride (80.66 mg, 658.20 mol, 2.0 eq.). The resulting mixture was stirred at 25° C. for 16 h. The solvent was removed in vacuo. The residue was dissolved in NaOH (2 M, 4.00 mL, 24.3 eq.) and stirred at 100° C. for 1 h. The mixture was diluted with water (10 mL) and extracted with DCM (50 mL×2). The combined organic phase was washed with brine (30 mL), dried over Na₂SO₄, filtered and concentrated in vacuo. The residue was purified with prep-TLC (DCM/MeOH=15/1). The desired product of 4-[[2-(2-methoxyethyl)-1H-imidazo[4,5-c]quinolin-9-yl]oxy]-2-methyl-butan-2-ol (90.00 mg, 273.23 μmol, 83.02% yield) was obtained as a brown solid. ¹H NMR (400 MHz, CD₃OD) δ ppm: 9.08; (s, 1H), 7.73; (d, J=8.4 Hz, 1H), 7.65; (t, J=8.0 Hz, 1H), 7.18; (d, J=7.2 Hz, 1H), 4.51; (t, J=6.0 Hz, 2H), 3.93; (t, J=6.4 Hz, 2H), 3.42; (s, 3H), 3.33-3.28; (m, 2H), 2.23; (t, J=6.0 Hz, 2H), 1.44; (s, 6H); ES-LCMS m/z: 330.3 [M+H]⁺.

Step 2: Synthesis of 4-[[2-(2-Methoxyethyl)-5-oxido-1H-imidazo[4,5-c]quinolin-5-ium-9-yl]oxy]2-methyl-butan-2-ol

To a solution of 4-[[2,-(2-methoxyethyl)-1H-imidazo[4,5-c]quinolin-9-yl]oxy]-2-methyl-butan-2-ol (90.00 mg, 273.23 mol, 1.0 eq.) in DCM (10.00 mL) was added m-CPBA (83.21 mg, 409.85 mol, 85% purity, 1.5 eq.). The resulting mixture was stirred at 25° C. for 0.5 h. The solvent was removed in vacuo. The residue was purified with prep-TLC (DCM/MeOH=15/1). The desired product of 4-[[2,-(2-methoxyethyl)-5-oxido-1H-imidazo[4,5-c]-quinolin-5-ium-9-yl]oxy]-2-methyl-butan-2-ol (60.00 mg, 173.72 mol, 63.58% yield) was obtained as a yellow solid. ¹H NMR (400 MHz, CDCl₃) δ ppm: 8.97; (s, 1H), 8.36; (d, J=8.8 Hz, 1H), 7.54; (t, J=8.4 Hz, 1H), 6.94; (d, J=8.0 Hz, 1H), 4.38; (t, J=5.6 Hz, 2H), 3.81; (t, J=6.2 Hz, 2H), 3.40; (s, 3H), 3.17; (t, J=6.0 Hz, 2H), 2.24; (t, J=5.6 Hz, 2H), 1.48; (s, 6H); ES-LCMS m/z: 345.9 [M+H]⁺.

Step 3: Synthesis of 4-[[4-Amino-2-(2-methoxyethyl)-1H-imidazo[4,5-c]quinolin-9-yl]oxy]-2-methyl-butan-2-ol

To a solution of 4-[[2,-(2-methoxyethyl)-5-oxido-1H-imidazo[4,5-c]quinolin-5-ium-9-yl]oxy]-2-methyl-butan-2-ol (60.00 mg, 173.72 mol, 1.0 eq.) and NH₃.H₂O (217.81 mg, 1.74 mmol, 239.35 μL, 28% purity, 10.0 eq.) in CHCl₃ (6.00 mL) was added TsCl (66.24 mg, 347.44 mol, 2.0 eq.). The resulting mixture was stirred at 25° C. for 0.5 h. The solvent was removed in vacuo. The residue was purified with prep-HPLC (MeCN/H₂O as eluents, acidic condition). After lyophilization, the desired product of 4-[[4-amino-2-(2-methoxyethyl)-1H-imidazo[4,5-c]quinolin-9-yl]oxy]-2-methyl-butan-2-ol (24.95 mg, 63.20 mol, 36.38% yield, 96.48% purity, as HCl salt) was obtained as a white solid. ¹H NMR (400 MHz, CD₃OD) δ ppm: 7.66 (t, J=8.2 Hz, 1H), 7.32; (d, J=8.0 Hz, 1H), 7.13; (d, J=8.0 Hz, 1H), 4.49; (t, J=6.0 Hz, 2H), 3.93; (t, J=6.6 Hz, 2H), 3.42; (s, 3H), 3.26; (t, J=6.2 Hz, 2H), 2.19; (t, J=5.8 Hz, 2H), 1.43; (s, 6H); ES-LCMS m/z: 345.3 [M+H]⁺.

Example 6

Synthesis of 4-[4-Amino-2-(ethoxymethyl)-1-methyl-imidazo[4,5-c]quinolin-9-yl]oxy-2-methyl-butan-2-ol

Step 1: Synthesis of 4-(methylamino)-3-nitro-quinolin-5-ol

To a solution of 5-methoxy-N-methyl-3-nitro-quinolin-4-amine (300.00 mg, 1.29 mmol, 1.0 eq.) in DCM (15.00 mL) was added BBr₃ (1.62 g, 6.45 mmol, 621.48 μL, 5.0 eq.) dropwise at −78° C. The resulting mixture was stirred at 60° C. for 2 h. The mixture was added to MeOH (100 mL) dropwise at −30° C. The solvent was removed in vacuo. The desired product of 4-(methylamino)-3-nitro-quinolin-5-ol (300.00 mg, crude) was obtained as a brown solid. ¹H NMR (400 MHz, CD₃OD) δ ppm: 9.22; (s, 1H), 7.79; (m, 1H), 7.33; (m, 1H), 7.15-7.13; (m, 1H), 3.08; (s, 3H); ES-LCMS m/z: 220.2 [M+H]⁺.

Step 2: Synthesis of 2-methyl-4-[[4-(methylamino)-3-nitro-5-quinolyl]oxy]butan-2-ol

To a solution of 4-(methylamino)-3-nitro-quinolin-5-ol (250.00 mg, 1.14 mmol, 1.0 eq.), TBAB (367.67 mg, 1.14 mmol, 1.0 eq.) and KI (189.32 mg, 1.14 mmol, 1.0 eq.) in NaOH (2 M, 1.71 mL, 3.0 eq.) was added a solution of (3-hydroxy-3-methyl-butyl)4- methylbenzenesulfonate (883.49 mg, 3.42 mmol, 3.0 eq.) in DCM (3.00 mL). The resulting mixture was stirred at 25° C. for 64 h. The reaction mixture was diluted with H₂O (10 mL) and extracted with DCM (30 mL×2). The combined organic layers were washed with brine (10 mL), dried over Na₂SO₄, filtered and concentrated under reduced pressure to give a residue. The residue was purified with column chromatography (DCM to DCM/MeOH=20/1). The desired product of 2-methyl-4[[4-(methylamino)-3-nitro-5-quinolyl]oxy]butan-2-ol (100.00 mg, 327.51 mol, 28.73% yield) was obtained as a yellow solid. ¹H NMR (400 MHz, CDCl₃) δ ppm: 9.36; (s, 1H), 9.02; (s, 1H), 7.61-7.55; (m, 2H), 6.91; (d, J=6.8 Hz, 1H), 4.36; (t, J=5.8 Hz, 2H), 2.84; (d, J=5.2 Hz, 3H), 2.13; (t, J=5.8 Hz, 2H), 1.41; (s, 6H); ES-LCMS m/z: 306.0 [M+H]⁺.

Step 3: Synthesis of 4-[[3-Amino-4-(methylamino)-5-quinolyl]oxy]-2-methyl-butan-2-ol

To a solution of 2-methyl-4[[4-(methylamino)-3-nitro-5-quinolyl]oxy]butan-2-ol (100.00 mg, 327.51 μmol, 1.0 eq.) in MeOH (50.00 mL) was added Raney-Ni (100.00 mg, 1.17 mmol, 3.6 eq.) under N₂. The suspension was degassed under vacuum and purged with H₂ several times. The mixture was stirred under H₂ (15 psi) at 25° C. for 1 h. The mixture was filtered. The filtrate was concentrated in vacuo. The desired product of 4-[[3-amino-4-(methylamino)-5-quinolyl]oxy]-2-methyl-butan-2-ol (80.00 mg, 290.54 μmol, 88.71% yield) was obtained as a green solid. ¹H NMR (400 MHz, CD₃OD) δ ppm: 8.07; (s, 1H), 7.44; (t, J=8.0 Hz, 1H), 7.29; (d, J=8.4 Hz, 1H), 6.95; (d, J=7.6 Hz, 1H), 4.35; (t, J=6.4 Hz, 2H), 3.19; (d, J=10.4 Hz, 3H), 2.10; (d, J=6.4 Hz, 2H), 1.33; (s, 6H); ES-LCMS m/z: 276.3 [M+H]⁺.

Step 4: Synthesis of 4-[2-(ethoxymethyl)-1-methyl-imidazo[4,5-c]quinolin-9-yl]oxy-2-methyl-butan-2 -ol

4-[[3-Amino-4-(methylamino)-5-quinolyl]oxy]-2-methyl-butan-2-ol (70.00 mg, 254.22 μmol, 1.0 eq.), 2-ethoxyacetic acid (1.65 g, 15.85 mmol, 1.50 mL, 62.4 eq.) and 4 Å MS (100.00 mg) were placed into a microwave tube. The sealed tube was heated at 120° C. for 30 minutes under microwave. The mixture was filtered. The filtrate was diluted with DCM (50 mL) and water (10 mL) and was adjusted to pH=7 by aqueous NaOH (2 M). The organic layer was separated and washed with brine (10 mL), dried with anhydrous Na₂SO₄, filtered and concentrated in vacuo. The crude product was purified with prep-TLC (DCM/MeOH=15/1). The desired product of 4-[2-(ethoxymethyl)-1-methyl-imidazo[4,5-c]quinolin-9-yl]oxy-2-methyl-butan-2-ol (20.00 mg, 58.24 μmol, 22.91% yield) was obtained as a yellow solid. ¹H NMR (400 MHz, CDCl₃) δ ppm: 9.25; (s, 1H), 7.88; (d, J=7.6 Hz, 1H), 7.59; (t, J=8.2 Hz, 1H), 7.10; (d, J=7.2 Hz, 1H), 4.89; (s, 2H), 4.48; (t, J=7.6 Hz, 2H), 4.32; (s, 3H), 3.66-3.61; (m, 2H), 2.20; (t, J=7.6 Hz, 2H), 1.38; (s, 6H), 1.26; (m, 3H); ES-LCMS m/z: 344.3 [M+H]⁺.

Step 5: Synthesis of 4-[2-(Ethoxymethyl)-1-methyl-5-oxido-imidazo[4,5-c]quinolin-5-ium-9-yl]oxy-2-methyl-butan-2-ol

To a solution of 4-[2-(ethoxymethyl)-1-methyl-imidazo[4,5-c]quinolin-9-yl]-oxy-2-methyl-butan-2-ol (20.00 mg, 58.24 μmol, 1.0 eq.) in DCM (5.00 mL) was added m-CPBA (23.65 mg, 116.48 mol, 85% purity, 2.0 eq.). The resulting mixture was stirred at 25° C. for 0.5 h. The solvent was removed in vacuo. The residue was purified with prep-TLC (DCM/MeOH=10/1). The desired product of 4-[2-(ethoxymethyl)-1-methyl-5-oxido-imidazo[4,5-c]quinolin-5-ium-9-yl]oxy-2-methyl-butan-2-ol (20.00 mg, crude) was obtained as a white solid. ¹H NMR (400 MHz, CDCl₃) δ ppm: 9.28; (s, 1H), 8.70; (d, J=8.8 Hz, 1H), 7.71; (t, J=8.2 Hz, 1H), 7.22; (d, J=8.0 Hz, 1H), 4.86; (s, 2H), 4.52-4.48; (m, 2H), 4.28; (s, 3H), 3.67-3.61; (m, 2H), 2.23-2.16; (m, 2H), 1.35; (s, 6H), 1.29-1.27; (m, 3H); ES-LCMS m/z: 360.3 [M+H]⁺.

Step 6: Synthesis of 4-[4-Amino-2-(ethoxymethyl)-1-methyl-imidazo [4,5-c]quinolin-9-yl]oxy-2-methyl-butan-2-ol

To a solution of 4-[2-(ethoxymethyl)-1-methyl-5-oxido-imidazo[4,5-c]quinolin-5-ium-9-yl]oxy-2-methyl-butan-2-ol (20.00 mg, 55.65 mol, 1.0 eq.) and NH₃.H₂O (69.66 mg, 556.45 mol, 76.54 μL, 28% purity, 10.0 eq.) in CHCl₃ (2.00 mL) was added TsCl (15.91 mg, 83.47 μmol, 1.5 eq.). The resulting mixture was stirred at 25° C. for 0.5 h. The solvent was removed in vacuo. The residue was purified with prep-HPLC (MeCN/H₂O as eluents, acidic condition). After lyophilization, the desired product of 4-[4-amino-2-(ethoxymethyl)-1 -methyl-imidazo[4,5-c]quinolin-9-yl]oxy-2- methyl-butan-2-ol (6.00 mg, 15.19 mol, 27.30% yield, as a HCl salt) was obtained as a white solid: ¹H NMR (400MHz, CD₃OD) δ ppm: 7.65; (t, J=8.2 Hz, 1H), 7.31; (d, J=8.4 Hz, 1H), 7.18; (d, J=8.0 Hz, 1H), 4.85; (s, 2H), 4.48; (t, J=7.8 Hz, 2H), 4.26; (s, 3H), 3.68-3.63; (m, 2H), 2.16; (t, J=7.8 Hz, 2H), 1.31; (s, 6H), 1.26; (t, J=6.8 Hz, 3H); ES-LCMS m/z: 359.3 [M+H]⁺.

The following compound was prepared in a similar way as that described in Examples 5 and 6 using corresponding reagents.

2-(Ethoxymethyl)-9-(2-isopropoxyethoxy)-1H-imidazo[4,5-c]quinolin-4-amine was obtained in 40.79% yield with 100% purity as a HCl salt as a white solid. ¹H NMR (400 MHz, CD₃OD) δ ppm: 7.63; (t, J=8.2 Hz, 1H), 7.30; (d, J=8.4 Hz, 1H), 7.18; (d, J=8.0 Hz, 1H), 4.79 (s, 2H), 4.54-4.51; (m, 2H), 3.94-3.91; (m, 2H), 3.75-3.69; (m, 1H), 3.66-3.64; (m, 2H), 1.24; (t, J=7.0 Hz, 3H), 1.15; (d, J=6.0 Hz, 6H) ; ES-LCMS m/z: 345.3 [M+H].

Example 7

Synthesis of 4[4-Amino-2-(ethoxymethyl)-1-isobutyl-imidazo[4,5-c]quinolin-9-yl]oxy-2-methyl-butan-2-ol

Step 1: Syntheis of 3-Amino-4-(isobutylamino)quinolin-5-ol

To a solution of N⁴-isobutyl-5-methoxy-quinoline-3,4-diamine (450.00 mg, 1.83 mmol, 1.0 eq.) in DCM (30.00 mL) was added BBr₃ (2.30 g, 9.17 mmol, 883.73 μL, 5.0 eq.) dropwise at −78° C. The resulting mixture was stirred at 60° C. for 2 h. The mixture was added to MeOH (100 mL) dropwise at −30° C. The solvent was removed in vacuo. The desired product of 3-amino-4-(isobutylamino) quinolin-5-ol (500.00 mg, 1.64 mmol, 89.81% yield, as 2HCl salt) was obtained as a brown solid. ¹H NMR (400 MHz, CD₃OD) δ ppm: 8.19; (s, 1H), 7.65; (t, J=8.2 Hz, 1H), 7.24; (d, J=8.4 Hz, 1H), 6.97; (d, J=7.2 Hz, 1H), 3.80; (d, J=6.4 Hz, 2H), 2.07-2.02; (m, 1H), 1.10; (d, J=6.4 Hz, 6H); ES-LCMS m/z: 232.3 [M+H]⁺.

Step 2: Synthesis of 2-(Ethoxymethyl)-1-isobutyl-imidazo[4,5-c]quinolin-9-ol

To a solution of 3-amino-4-(isobutylamino)quinolin-5-ol (450.00 mg, 1.48 mmol, 1.0 eq., as 2HCl salt) in Pyridine (4.90 g, 61.95 mmol, 5.0 mL, 41.9 eq.) was added 2-ethoxyacetyl chloride (271.92 mg, 2.22 mmol, 1.5 eq.). The resulting mixture was stirred at 25° C. for 1 h. The solvent was removed in vacuo. The residue was dissolved in NaOH (2 M, 7.40 mmol, 3.0 mL, 5.0 eq.) and stirred at 100° C. for 2 h. The mixture was partitioned between DCM (40 mL) and water (10 mL). The organic layer was separated, washed with brine (10 mL), dried over Na₂SO₄, filtered and concentrated in vacuo. The residue was purified with column chromatography (DCM to DCM/MeOH=10/1). The desired product of 2-(ethoxymethyl)-1-isobutyl-imidazo[4,5-c]quinolin-9-ol (100.00 mg, 334.03 mol, 22.58% yield) was obtained as a red solid. ¹H NMR (400 MHz, CD₃OD) δ ppm: 9.06; (s, 1H), 7.69-7.67; (m, 1H), 7.56; (t, J=8.0 Hz, 1H), 7.11-7.08; (m, 1H), 4.89; (s, 2H), 4.65-4.63; (m. 2H), 3.68-3.62; (m, 2H), 2.24-2.16; (m, 1H), 1.26; (t, J=7.0 Hz, 3H), 0.79-0.76; (m, 6H); ES-LCMS m/z: 300.3 [M+H]⁺.

Step 3: Synthesis of 4-[2-(Ethoxymethyl)-1-isobutyl-imidazo[4,5-c]quinolin-9-yl]oxy-2-methyl-butan-2-ol

To a solution of 2-(ethoxymethyl)-1-isobutyl-imidazo[4,5-c]quinolin-9-ol (60.00 mg, 200.42 mol, 1.0 eq.), TBAB (64.61 mg, 200.42 mol, 1.0 eq.) and KI (33.27 mg, 200.42 mol, 1.0 eq.) in NaOH (2 M, 300.63 μL, 3.0 eq.) was added a solution of (3-hydroxy-3-methyl-butyl)4-methylbenzenesulfonate (155.32 mg, 601.26 mol, 3.0 eq.) in DCM (3.00 mL). The resulting mixture was stirred at 25° C. for 64 h. The reaction mixture was diluted with H₂O (20 mL) and extracted with DCM (50 mL×2). The combined organic layers were washed with brine (20 mL), dried over Na₂SO₄, filtered and concentrated under reduced pressure to give a residue. The residue was purified with column chromatography (DCM to DCM/MeOH=10/1). The desired product of 4-[2-(ethoxymethyl)-1-isobutyl-imidazo[4,5-c]quinolin-9-yl]oxy-2-methyl-butan-2-ol (60.00 mg, 155.64 mol, 77.66% yield) was obtained as a red solid. ¹H NMR (400 MHz, CDCl₃) δ ppm: 9.26; (s, 1H), 7.88; (d, J=8.4 Hz, 1H), 7.59; (t, J=8.2 Hz, 1H), 7.09; (d, J=7.2 Hz, 1H), 4.88; (s, 2H), 4.68; (br, s. 2H), 4.48; (t, J=7.4 Hz, 2H), 3.65-3.59; (m, 2H), 2.19; (t, J=7.6 Hz, 2H), 2.06-2.02; (m, 1H), 1.34; (s, 6H), 1.28-1.24; (m, 3H), 0.66; (d, J=6.0 Hz, 6H); ES-LCMS m/z: 386.4 [M+H]⁺.

Step 4: Synthesis of 4-[2-(Ethoxymethyl)-1-isobutyl-5-oxido-imidazo[4,5-c]quinolin-5-ium-9-yl]oxy-2-methyl-butan-2-ol

To a solution of 4-[2-(ethoxymethyl)-1-isobutyl-imidazo[4,5-c]quinolin-9-yl]oxy-2-methyl-butan-2-ol (60.00 mg, 155.64 mol, 1.0 eq.) in DCM (10.00 mL) was added m-CPBA (47.40 mg, 233.46 mol, 85% purity, 1.5 eq.). The resulting mixture was stirred at 25° C. for 0.5 h. The solvent was removed in vacuo. The residue was purified with prep-TLC (DCM/MeOH=10/1). The desired product of 4-[2-(ethoxymethyl)-1-isobutyl-5-oxido-imidazo[4,5-c]quinolin-5-ium-9-yl]oxy-2-methyl-butan-2-ol (50.00 mg, 124.53 mol, 80.01% yield) was obtained as a yellow solid. ¹HNMR (400 MHz, CDCl₃) δ ppm: 9.07; (s, 1H), 8.68; (d, J=8.0 Hz, 1H), 7.68; (t, J=8.4 Hz, 1H), 7.22; (d, J=8.0 Hz, 1H), 4.84; (s, 2H), 4.61; (br, s. 2H), 4.51; (t, J=7.8 Hz, 2H), 3.65-3.59; (m, 2H), 2.19; (t, J=7.6 Hz, 2H), 1.99-1.94; (m, 1H), 1.35; (s, 6H), 1.29-1.27; (m, 3H), 0.67; (d, J=6.0 Hz, 6H); ES-LCMS m/z: 402.4 [M+H]⁺.

Step 5: Synthesis of 4-[4-Amino-2-(ethoxymethyl)-1-isobutyl-imidazo[4,5-c]quinolin-9-yl]oxy-2-methyl-butan-2-ol

To a solution of 4-[2-(ethoxymethyl)-1-isobutyl-5-oxido-imidazo[4,5-c]quinolin-5-ium-9-yl]oxy-2-methyl-butan-2-ol (50.00 mg, 124.53 mol, 1.0 eq.) and NH₃.H₂O (155.89 mg, 1.25 mmol, 171.31 μL, 28% purity, 10.0 eq.) in CHCl₃ (5.00 mL) was added TsCl (28.49 mg, 149.44 mol, 1.2 eq.). The resulting mixture was stirred at 25° C. for 0.5 h. The solvent was removed in vacuo. The residue was purified with prep-HPLC (MeCN/H₂O as eluents, acidic condition). After lyophilization, the desired product of 4-[4-amino-2-(ethoxymethyl)-1-isobutyl-imidazo[4,5-c]quinolin-9-yl]oxy-2-methyl-butan-2-ol (26.50 mg, 60.38 μmol, 48.48% yield, 99.56% purity, as a HCl salt) was obtained as a white solid. ¹H NMR (400 MHz, CD₃OD) δ ppm: 7.69; (t, J=8.2 Hz, 1H), 7.34; (t, J=8.0 Hz, 1H), 7.22; (d, J=8.4 Hz, 1H), 4.87; (s, 2H), 4.71; (br, s. 2H), 4.53; (t, J=7.6 Hz, 1H), 3.69-3.63; (m, 2H), 2.18; (t, J=7.6 Hz, 2H), 2.02-1.97; (m, 1H), 1.29; (s, 6H), 1.26; (t, J=7.0 Hz, 3H), 0.74; (d, J=4.2 Hz, 6H); ES-LCMS m/z: 401.4 [M+H]⁺.

Example 8

Preparation of Intermediates

Intermediate 1: 4-Chloro-5 -methoxy-3 -nitro-quinoline

Step 1: Synthesis of 2-methoxy-6-[[(E)-2-nitrovinyl]amino]benzoic acid

To a solution of NaOH (40.20 g, 1.01 mol, 3.4 eq.) in water (100 mL) was added CH₃NO₂ (23.73 g, 388.84 mmol, 21.00 mL, 1.3 eq.) at 0° C. The mixture was warmed to 40° C. and additional amount of CH₃NO₂ (23.73 g, 388.84 mmol, 21.00 mL, 1.3 eq.) was added slowly at 40° C. This temperature was maintained until all solids dissolved and a clear red solution was obtained. The solution was cooled to 30° C., poured into 300 g of chipped ice, and acidified with concentrated HCl (100 mL). The mixture was immediately added to a solution of 2-amino-6-methoxy-benzoic acid (50.00 g, 299.11 mmol, 1.0 eq.) and conc. HCl (35 mL) in water (1400 mL). The solution was allowed to stir at 20° C. for 16 h. The mixture was filtered. The cake was washed with water (300 mL×3), and dried in vacuo. The desired product of 2-methoxy-6-[[(E)-2-nitrovinyl]amino]benzoic acid (67.00 g, 281.28 mmol, 94.04% yield) was obtained as a yellow solid. ¹H NMR (400 MHz, CD₃OD) δ ppm: 7.70; (d, J=6.0 Hz, 1H), 7.51; (t, J=8.4 Hz, 1H), 7.11; (d, J=8.4 Hz, 1H), 6.93; (d, J=8.4 Hz, 1H), 6.68; (d, J=6.0 Hz, 1H), 3.89 (d, J=4.4 Hz, 3H); ES-LCMS m/z: 261.1 [M+Na]⁺.

Step 2: Synthesis of 5-methoxy-3-nitro-quinolin-4-ol

A solution of 2-methoxy-6-[[(E)-2-nitrovinyl]amino]benzoic acid (56.00 g, 235.10 mmol, 1.0 eq.) in Ac₂O (300.00 mL) was heated at 105° C. for 0.5 h, and a clear solution was obtained. AcOK (27.69 g, 282.12 mmol, 1.2 eq.) was added. The resulting mixture was stirred at 105° C. for 2 h. The mixture was filtered. The cake was washed with acetic acid (30 mL×2) and water (100 mL×3). The cake was dried on oil pump. The desired product of 5-methoxy-3-nitro-quinolin-4-ol (19.00 g, 86.29 mmol, 36.70% yield) was obtained as an off-white solid. ¹H NMR (400 MHz, DMSO-d₆) δ ppm: 12.59; (s, 1H), 8.96; (s, 1H), 7.62; (t, J=8.2 Hz, 1H), 7.16; (d, J=8.0 Hz, 1H), 6.95; (d, J=8.0 Hz, 1H), 3.83; (s, 3H); ES-LCMS m/z: 221.2 [M+H]⁺.

Step 3: Synthesis of 4-chloro-5-methoxy-3-nitro-quinoline

To a suspension of 5-methoxy-3-nitro-quinolin-4-ol (2.00 g, 9.08 mmol, 1.0 eq.) in SOCl₂ (8.20 g, 68.92 mmol, 5.00 mL, 7.6 eq.) was added DMF (66.39 mg, 908.35 μmol, 69.89 μL, 0.1 eq.). The resulting mixture was stirred at 80° C. for 4 h. The solvent was removed in vacuo. The desired product of 4-chloro-5-methoxy-3-nitro-quinoline (2.10 g, 8.80 mmol, 96.92% yield) was obtained as a brown solid. ¹H NMR (400 MHz, CDCl₃) δ ppm: 9.12; (s, 1H), 8.08; (t, J=8.8 Hz, 1H), 7.96-7.92; (m, 1H), 7.20; (d, J=8.4 Hz, 1H), 4.08; (s, 3H); ES-LCMS m/z: 239.2 [M+H]⁺.

Intermediate 2: 4-Amino-3-nitro-quinolin-5-ol

Step 1: Synthesis of 5-methoxy-3-nitro-quinolin-4-amine

A solution of 4-chloro-5-methoxy-3-nitro-quinoline (5.28 g, 22.13 mmol, 1.0 eq.) in THF (50 mL) was added to NH₃.H₂O (91.00 g, 726.96 mmol, 100.00 mL, 28% purity, 32.9 eq.) in THF (100 mL) dropwise at 0° C. The mixture was stirred at 25° C. for 2 h. The reaction mixture was filtered. The residue was washed with H₂O (50 mL×3) and dried in vacuo. The desired product of 5-methoxy-3-nitro-quinolin-4-amine (4.83 g, 22.03 mmol, 99.55% yield) was obtained as a yellow solid. ¹H NMR (400 MHz, CD₃OD) δ ppm: 9.17; (s, 1H), 7.75; (t, J=8.4 Hz, 1H), 7.46; (d, J=8.4 Hz, 1H), 7.15; (d, J=8.0 Hz, 1H), 4.13; (s, 3H); ES-LCMS m/z: 220.2 [M+H]⁺.

Step 2: Synthesis of 4-amino-3-nitro-quinolin-5-ol

To a solution of 5-methoxy-3-nitro-quinolin-4-amine (2.00 g, 9.12 mmol, 1.0 eq.) in DCM (100.00 mL) was added BBr₃ (22.86 g, 91.20 mmol, 8.79 mL, 10.0 eq.) dropwise at −78° C. The reaction mixture was stirred at 60° C. for 16 h. The reaction mixture was added to MeOH (200 mL) at −30° C., and then concentrated under reduced pressure to give a residue. The residue was suspended in DCM and filtered. The cake was dried in vacuo. The desired product of 4-amino-3-nitro-quinolin-5-ol (2.53 g, crude) was obtained as a green solid. ¹H NMR (400 MHz, CD₃OD) δ ppm: 9.41; (s, 1H), 7.83; (t, J=8.4 Hz, 1H), 7.33; (d, J=8.4 Hz, 1H), 7.13; (d, J=8.4 Hz, 1H); ES-LCMS m/z: 206.2 [M+H]⁺.

Intermediate 3: N⁴-Isobutyl-5-methoxy-quinoline-3,4-diamine

Step 1: Synthesis of N-isobutyl-5-methoxy-3-nitro-quinolin-4-amine

To a solution of 2-methylpropan-1-amine (612.91 mg, 8.38 mmol, 828.26 μL, 2.0 eq.) and Et₃N (2.12 g, 20.95 mmol, 2.90 mL, 5.0 eq.) in DCM (50.00 mL) was added 4-chloro-5-methoxy-3-nitro-quinoline (1.00 g, 4.19 mmol, 1.0 eq.). The resulting mixture was stirred at 25° C. for 0.5 h. The reaction mixture was washed with water (30 mL) and brine (30 mL) via extraction. The organic phase was dried over anhydrous Na₂SO₄, filtered and concentrated in vacuo. The residue was purified with column chromatography (PE to PE/EtOAc=1/1). The desired product of N-isobutyl-5-methoxy-3-nitro-quinolin-4-amine (1.00 g, 3.63 mmol, 86.69% yield) was obtained as a yellow solid. ¹H NMR (400 MHz, CD₃OD) ppm: 8.85; (s, 1H), 7.70; (t, J=8.2 Hz, 1H), 7.47; (d, J=7.6 Hz, 1H), 7.16; (d, J=8.0 Hz, 1H), 4.14; (s, 3H), 2.85; (d, J=6.4 Hz, 2H), 2.04-1.94; (m, 1H), 1.00; (d, J=6.8 Hz, 6H); ES-LCMS m/z: 276.2 [M+H]⁺.

Step 2: Synthesis of N⁴-isobutyl-5-methoxy-quinoline-3,4-diamine

To a solution of N-isobutyl-5-methoxy-3-nitro-quinolin-4-amine (300.00 mg, 1.09 mmol, 1.0 eq.) in MeOH (50.00 mL) was added Raney-Ni (100.00 mg, 1.17 mmol, 1.1 eq.) under N₂. The suspension was degassed under vacuum and purged with H₂ several times. The mixture was stirred under H₂ (15 psi) at 25° C. for 1 h. The reaction mixture was filtered. The filtrate was concentrated in vacuo. The desired product of N⁴-isobutyl-5-methoxy-quinoline-3,4-diamine (250.00 mg, 1.02 mmol, 93.49% yield) was obtained as a yellow solid. ¹H NMR (400 MHz, CD₃OD) δ ppm: 8.28; (s, 1H), 7.42-7.40; (m, 1H), 7.33; (t, J=8.2 Hz, 1H), 6.91; (d, J=7.6 Hz, 1H), 4.03; (s, 3H), 3.08; (d, J=6.8 Hz, 2H), 1.90-1.80; (m, 1H), 1.02; (d, J=6.8 Hz, 6H); ES-LCMS m/z: 246.3 [M+H]⁺.

Intermediate 4: 4-[3,4-Diamino-5-quinolyl)oxy]-2-methyl-butan-2-ol

Step 1: Synthesis of 4-[(4-amino-3-nitro-5-quinolyl)oxy]-2-methyl-butan-2-ol

To a solution of 4-amino-3-nitro-quinolin-5-ol (1.50 g, 7.31 mmol, 1.0 eq.), TBAB (2.36 g, 7.31 mmol, 1.0 eq.) and KI (405.04 mg, 2.44 mmol, 1.0 eq.) in NaOH (2 M, 3.66 mL, 3.0 eq.) was added a solution of (3-hydroxy-3-methyl-butyl)4-methylbenzenesulfonate (5.67 g, 21.93 mmol, 3.0 eq.) in DCM (15.00 mL). The resulting mixture was stirred at 25° C. for 64 h. The reaction mixture was diluted with H₂O (10 mL) and extracted with DCM (50 mL×2). The combined organic layers were washed with brine (10 mL), dried over anhydrous Na₂SO₄, filtered and concentrated under reduced pressure to give a residue. The residue was purified with column chromatography (SiO₂, DCM/MeOH=100/1 to 20/1). The desired product of 4-[(4-amino-3-nitro-5-quinolyl)oxy]-2-methyl-butan-2-ol (646.00 mg, 2.22 mmol, 30.34% yield) was obtained as a yellow solid. ¹H NMR (400 MHz, CDCl₃) δ ppm: 9.59; (br s, 1H), 9.29; (s, 1H), 9.22; (br s, 1H), 7.63; (t, J=8.2 Hz, 1H), 7.54; (dd, J=8.4, 0.8 Hz, 1H), 6.92; (d, J=7.6 Hz, 1H), 4.38; (t, J=6.2 Hz, 2H), 2.14; (t, J=6.2 Hz, 2H), 1.41; (s, 6H); ES-LCMS m/z: 292.3 [M+H]⁺.

Step 2: Synthesis of 4-[(3, 4-diamino-5-quinolyl)oxy]-2-methyl-butan-2-ol

To a solution of 4-[(4-amino-3-nitro-5-quinolyl)oxy]-2-methyl-butan-2-ol (640.00 mg, 2.20 mmol, 1.0 eq.) in MeOH (150.00 mL) was added Raney-Ni (200.00 mg, 2.33 mmol, 1.1 eq.) under N₂. The suspension was degassed under vacuum and purged with H₂ several times. The mixture was stirred under H₂ (15 psi) at 25° C. for 1 h. The reaction mixture was filtered. The filtrate was concentrated under reduced pressure to give a residue. The product was directly used in the next step without further purification. The desired crude product of 4-[(3,4-diamino-5-quinolyl) oxy]-2-methyl-butan-2-ol (570.00 mg, 2.18 mmol, 99.15% yield) was obtained as a black brown solid. ¹H NMR (400 MHz, CDCl₃) δ ppm: 8.24; (s, 1H), 7.47; (d, J=8.4 Hz, 1H), 7.30; (t, J=8.0 Hz, 1H), 6.68; (d, J=7.6 Hz, 1H), 5.89; (br s, 2H), 4.28; (t, J=6.4 Hz, 2H), 2.11; (t, J=6.4 Hz, 2H), 1.36; (s, 6H); ES-LCMS m/z: 262.2 [M+H].

Intermediate 5: 5 -Methoxy-N-methyl-3 -nitro-quinolin-4-amine

A solution of 4-chloro-5-methoxy-3-nitro-quinoline (1.00 g, 4.19 mmol, 1.0 eq.) in DCM (30.00 mL) was added to MeNH₂ (2 M in THF, 40.00 mL, 19.1 eq.). The mixture was stirred at 25° C. for 2 h. The mixture was concentrated to give a residue. The residue was purified with column chromatography (SiO₂, DCM/MeOH=50/1 to 20/1). The desired product of 5-methoxy-N-methyl-3-nitro-quinolin-4-amine (400.00 mg, 1.72 mmol, 40.93% yield) was obtained as a yellow solid. ¹H NMR (400 MHz, CDCl₃) δ ppm: 9.03; (s, 1H), 8.79; (s, 1H), 7.62-7.60; (m, 2H), 6.94-6.92; (m, 1H), 4.09; (s, 3H), 2.94; (d, J=5.6 Hz, 3H); ES-LCMS m/z: 234.0 [M+H]⁺.

Intermediate 6: 2-Ethoxyacetyl chloride

To a solution of 2-ethoxyacetic acid (1.00 g, 9.61 mmol, 909.09 μL, 1.0 eq.) and catalytic amount of DMF (10.00 mg, 136.82 μmol, 10.53 μL, 0.01 eq.) in DCM (30.00 mL) was added oxalyl chloride (1.83 g, 14.41 mmol, 1.26 mL, 1.5 eq.) at 0° C. The resulting mixture was stirred at 25° C. for 2 h. The reaction mixture was concentrated under reduced pressure to remove the solvent. 2-Ethoxyacetyl chloride (900.00 mg, 7.34 mmol, 76.42% yield) was obtained as yellow oil.

Intermediate 7: 3-Methoxypropanoyl chloride

3-Methoxypropanoyl chloride was prepared in the same way as intermediate 6 using the corresponding starting material of 3-methoxypropanoic acid in 84.9% yield as yellow oil.

Intermediate 8: (3-Hydroxy-3-methyl-butyl) 4-methylbenzenesulfonate

To a solution of 3-methylbutane-1,3-diol (10.00 g, 96.02 mmol, 10.20 mL, 1.0 eq.), Et₃N (14.57 g, 144.03 mmol, 19.96 mL, 1.5 eq.) and DMAP (14.08 g, 115.22 mmol, 1.2 eq.) in DCM (200.00 mL) was added a solution of TsCl (17.39 g, 91.22 mmol, 0.95 eq) in DCM (100 mL) dropwise at 0° C. The resulting mixture was stirred at 0° C. for 1 h. The mixture was adjusted to pH=6 with citric acid. The organic layer was separated and washed with brine (100 mL), dried over anhydrous Na₂SO₄, filtered and concentrated in vacuo. (3-Hydroxy-3-methyl-butyl)4-methylbenzenesulfonate (19.80 g, 76.65 mmol, 79.83% yield) was obtained as a colorless oil. ¹H NMR (400 MHz, CDCl₃) δ ppm: 7.80-7.78; (m, 2H), 7.34; (d, J=8.0 Hz, 2H), 4.22-4.19; (m, 2H), 2.45; (s, 3H), 1.87-1.84; (m, 2H), 1.21; (d, J=1.2 Hz, 6H); ES-LCMS m/z: 276.2 [M+H₂O]⁺.

Intermediate 9: Isopentyl 4-methylbenzenesulfonate

Isopentyl 4-methylbenzenesulfonate was prepared in a similar way as intermediate 8 using the corresponding starting material of 3-methylbutan-1-ol and purified with silica gel chromatography (PE/EA=20/1 to 10/1) to give 72.76% isolated yield as a yellow oil. ¹H NMR (400 MHz, CDCl₃) δ ppm: 7.81-7.79; (m, 2H), 7.35; (d, J=8.0 Hz, 2H), 4.06; (t, J=6.6 Hz, 2H), 2.46; (s, 3H), 1.70-1.67; (m, 1H), 1.57-1.51; (m, 2H), 0.88-0.84; (m, 6H); ES-LCMS m/z: 264.9 [M+Na]⁺.

Intermediate 10: 2-Isopropoxyethyl 4-methylbenzenesulfonate

2-Isopropoxyethyl 4-methylbenzenesulfonate was prepared in a similar way as intermediate 8 using the corresponding starting material of 2-isopropoxyethanol in 81.44% yield as a colorless oil. ¹H NMR (400 MHz, CDCl₃) δ ppm: 7.80; (d, J=8.0 Hz, 2H), 7.33; (d, J=8.4 Hz, 2H), 4.14-4.11; (m, 2H), 3.60-3.58; (m, 2H), 3.55-3.54; (m, 1H), 2.44; (s, 3H), 1.08; (d, J=6.0 Hz, 6H); ES-LCMS m/z: 259.3 [M+H]⁺.

Intermediate 11: 3-Hydroxybutyl 4-methylbenzenesulfonate

3-Hydroxybutyl 4-methylbenzenesulfonate was prepared in a similar way as intermediate 8 using the corresponding starting material of butane-1,3-diol in 59.04% yield as a colorless oil. ¹H NMR (400 MHz, CDCl₃) δ ppm: 7.83-7.79; (m, 2H), 7.37-7.34; (m, 2H), 4.26-4.22; (m, 1H), 4.15-4.12; (m, 1H), 3.98-3.93; (m, 1H), 2.46; (s, 3H), 1.85-1.81; (m, 1H), 1.74-1.68; (m, 1H), 1.20; (m, 3H); ES-LCMS m/z: 245.2 [M+H]⁺.

Intermediate 12: Acetonyl 4-methylbenzenesulfonate:

Acetonyl 4-methylbenzenesulfonate was prepared in a similar way as intermediate 8 using the corresponding starting material of 1-hydroxypropan-2-one in 25.31% yield as a colorless oil. ¹H NMR (400 MHz, CDCl₃) δ ppm: 7.82; (d, J=8.4 Hz, 2H), 7.37; (d, J=8.4 Hz, 2H), 4.48; (s, 2H), 2.46; (s, 3H), 2.22; (s, 3H); ES-LCMS m/z: 229.2 [M+H]⁺.

Other 2-aminoquinoline derivatives were prepared in a similar way as that described in Examples 1-7, and they are listed in Table 1. These compounds were prepared in HCl salt forms, and/or in the forms of neutral amine. A person skilled in the art can clearly understand and know that the other analogs could be prepared by the same or similar methods as described in Examples 1-7. These examples are not in any way to limit the analogs that can be made by applying the same or similar methods presented herein.

TABLE 1 2-Amino-Quinoline Derivatives Prepared Cmpd No. Structure  1

 2

 3

 4

 5

 6

 7

 8

 9

10

11

12

13

14

15

16

17

18

19

20

21

22

23

24

25

26

27

28

29

30

31

32

33

34

35

36

37

38

39

40

41

42

43

44

45

46

47

The compound functionality was tested for some of the compounds prepared by stimulation and determination of cytokine production in PBMCs.

Human PBMCs were prepared from buffy coat obtained from healthy volunteer donor by Ficoll centrifugation and were adjusted to the final cell concentration to 1×10⁶ cells/mL.

For evaluation of compound activities, 1×10⁵ PBMCs were plated in a 96-well plate in 100 μl of RPMI 1640 complete medium (cat no. 31800-022, GIBCO by Life Technologies, Grand Island, N.Y., USA) supplemented with 10% fetal bovine serum, the tested compound was first dissolved in DMSO and further diluted in PBS and RPMI 1640 medium to the final concentration of 2004 (corresponding to 6.28 μg/mL), then 3-fold serially dilution was made in a 96-well round-bottom plate. 100 μl diluted compound was added to the same volume of 1×10⁵ PBMCs plate and cultured for 20-22 hours at 37° C. in a humidified atmosphere of 5% CO₂. The supernatant was collected for human IFN-α, IL12(p70) and IL-6 analysis by ELISA assay according to the manufacturer's instructions (Mabtech AB, Sweden). Resiquimod was used as a positive control.

Table 2 below lists the testing results on the evaluation of cytokine production for most of the compounds prepared.

TABLE 2 Compound Production of IFNa Production of IL-6 No. Structure M.W. on PBMC* on PBMC*  1

344.41 + +  2

328.41 + +  3

344.41 − −  4

330.38 − −  5

344.41 + +  6

328.41 N/A +  7

330.38 N/A +  8

316.35 + +  9

344.41 N/A + 10

358.43 N/A + 11

344.41 + + 12

400.51 + + 13

358.43 + + 14

358.43 + + 15

314.38 + + 16

358.43 + + 17

342.44 + + 18

328.41 + + 19

407.49 + + 20

437.51 + + 22

421.51 + + 23

595.86 + + 24

385.46 + + 25

609.89 + + 27

342.39 + + 28

341.41 + + 29

355.43 + + 31

270.33 − − 32

340.46 − − 33

326.44 − + 34

567.81 + + 35

581.83 + + 36

329.40 + + 37

314.38 + + 38

344.41 + + 39

284.31 + + 40

342.39 N/A − 41

342.39 N/A + 42

328.37 + + 43

328.37 N/A − 44

314.34 N/A − 45

314.34 N/A + 46

312.32 N/A + *Note 1: All the compounds were tested at concentration of 10 μM. Note 2: “+” means that there was production of IFNa or IL-6 on PBMC; while “−” means that no production of IFNa or IL-6 on PBMC was detected. 

What is claimed is:
 1. A compound represented by a formula:

or a salt thereof; wherein a dashed line represents the presence or absence of a bond; A¹ is CR¹, NR^(1A), or N; A² is CR²; B¹ is CR⁵ or N; B² is CR⁶ or N; B³ is CR⁷ or N; R¹ and R² are independently F, Cl, Br, I, NO₂, CN, R^(a), —OR^(a), —NR^(a)R^(b), —NHCOR^(a), —NHSO₂R^(a), —OCOR^(a), or —SO₂R^(a); X is a bond, O, NR^(a), —CO—, —SO—, or —SO₂—, —CONR^(a), hydrocarbyl, and R³ is H or C₁₋₃₀ organyl; or X-R³ is F or Cl; R^(1A), R⁴, R^(a), and R^(b) are independently H or C₁₋₃₀ organyl; R⁵, R⁶, and R⁷ are independently F, Cl, Br, I, NO₂, —CO₂R^(a), —CONR^(a)R^(b), CN, R^(a), —OR^(a), —NR^(a)R^(b), —NHCOR^(a), —NHSO₂R^(a), —OCOR^(a), —SO₂R^(a), —SO₂NHR^(a), or —X¹—(C_(m)H_(2m)O₀₋₁)—Z—(C_(n)H_(2n+1)), —(C_(m)H_(2m)O₀₋₁)—Z—(C_(n)H_(2n+1)), wherein R⁵ and R⁶ or R⁶ and R⁷ can be optionally linked to form a ring; wherein X¹ is a bond, O, NR^(a), —CO—, —SO—, or —SO₂—; Z is a bond, O, NHSO₂, or NHCO; m is 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10; and n is 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, or
 23. 2. The compound of claim 1, further represented by a formula:

or a salt thereof; wherein R⁴ is H, C₁₋₃₀ non-aromatic organyl, or C₁₋₃₀ aromatic organyl containing an aromatic group that is not directly attached to the N atom.
 3. The compound of claim 1 wherein R¹ or R^(1A) is C₁₋₁₂ optionally substituted alkyl.
 4. The compound of claim 3, wherein R¹ or R^(1A) is —C_(r)H_(2r+1)O, or an ester thereof, wherein r is 1, 2, 3, 4, 5, 6, 7, 8, 9, or
 10. 5. The compound of claim 4, wherein R¹ or R^(1A) is —C₃H₇O.
 6. The compound of claim 5, wherein R¹ or R^(1A) is —CH₂OCH₂CH₃.
 7. The compound of claim 1, wherein R² is H or C₁₋₁₂ optionally substituted alkyl.
 8. The compound of claim 7, wherein R² is C₁₋₆ alkyl, or —C_(y)H_(2y+1)O or an ester thereof, wherein y is 1, 2, 3, 4, 5, 6, 7, 8, 9, or
 10. 9. The compound of claim 8, wherein R² is CH₃.
 10. The compound of claim 7, wherein R² is H.
 11. The compound of claim 7, wherein R² is C₄H₉.
 12. The compound of claim 1, wherein R³ is C₁₋₃₀ optionally substituted alkyl.
 13. The compound of claim 12, wherein R³ is C₁₋₁₀ alkyl, or —C_(w)H_(2w+1)O or an ester thereof, wherein w is 1, 2, 3, 4, 5, 6, 7, 8, 9, or
 10. 14. The compound of claim 1, wherein R³ is —(C_(t)H_(wt)O₀₋₁)Ht, wherein t is 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10, and Ht is optionally substituted C₃₋₆ heterocyclyl.
 15. The compound of claim 1, wherein R³ is —(C_(u)H_(2u)O₀₋₁)—Z—(C_(v)H_(2v+1)), wherein Z is a bond, O, NHSO₂, or NHCO, u is 0, 1, 2, 3, 4, 5, or 6, and v is 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, or
 23. 16. The compound of claim 1, wherein R³ is —(C_(u)H_(2u)O₀₋₁)—NR^(a)R^(b), and u is 1, 2, 3, 4, 5, or 6, wherein R^(a) and R^(b) are independently H or C₁₋₆ alkyl.
 17. The compound of claim 13, wherein R³ is C₅H₁₁O.
 18. The compound of claim 17, wherein R³ is —CH₂—CH₂—C(CH₃)₂OH.
 19. The compound of claim 16, wherein R³ is —CH₂—CH₂—CH₂—NH₂.
 20. The compound of claim 1, wherein R⁴ is H or C₁₋₆ alkyl.
 21. The compound of claim 20, wherein R⁴ is H.
 22. The compound of claim 1, wherein R⁵ is R^(a), F, Cl, —CO₂R^(a), —CONR^(a)R^(b), CN, —OR^(a), —NR^(a)R^(b), —OCOR^(a), or —SO₂R^(a), —SO₂NHR^(a), wherein R^(a) and R^(b) are independently H or C₁₋₆ alkyl.
 23. The compound of claim 22, wherein R⁵ is H.
 24. The compound of claims 1, wherein R⁵ is —(C_(m)H_(2m)O₀₋₁)—Z—(C_(n)H_(2n+1)), wherein Z is a bond, O, NHSO2, or NHCO, m is 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10, and n is 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, or
 23. 25. The compound of claim 1, wherein R⁶ is R^(a), F, Cl, —CO₂R^(a), —CONR^(a)R^(b), CN, —OR^(a), —NR^(a)R^(b), —OCOR^(a), or —SO₂R^(a), —SO₂NHR^(a), wherein R^(a) and R^(b) are independently H or C₁₋₆ alkyl.
 26. The compound of claim 25, wherein R⁶ is H.
 27. The compound of claim 1, wherein R⁶ is —(C_(m)H_(2m)O₀₋₁)—Z—(C_(n)H_(2n+1)), wherein Z is a bond, O, NHSO₂, or NHCO, m is 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10, and n is 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, or
 23. 28. The compound of claim 1, wherein R⁷ is R^(a), F, Cl, —CO₂R^(a), —CONR^(a)R^(b), CN, —OR^(a), —NR^(a)R^(b), —OCOR^(a) , or —SO₂R^(a), —SO₂NHR^(a), wherein R^(a) and R^(b) are independently H or C₁₋₆ alkyl.
 29. The compound of claim 29, wherein R⁷ is H.
 30. The compound of claims 1, wherein R⁷ is —(C_(m)H_(2m)O₀₋₁)—Z—(C_(n)H_(2n+1)), wherein Z is a bond, O, NHSO₂, or NHCO, m is 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10, and n is 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, or
 23. 31. The compound of claim 1, R⁸ is H, OH, or CH₃.
 32. The compound of claim 31, wherein R⁸ is OH.
 33. The compound of claim 31, wherein R⁸ is H.
 34. A compound, which is:


35. The compound of claim 1 which is optionally substituted 9-methoxy-2H-pyrazolo[3,4-c]quinolin-4-amine.
 36. The compound of claim 1 which is optionally substituted 4-amino-2H-pyrazolo[3,4-c]quinolin-9-ol or a salt thereof; optionally substituted 4-amino-2-isopentyl-2H-pyrazolo[3,4-c]quinolin-9-ol or a salt thereof; optionally substituted 2-isopentyl-9-(isopentyloxy)-2H-pyrazolo[3,4-c]quinolin-4-amine or a salt thereof; or optionally substituted 2-butyl-9-(isopentyloxy)-2H-pyrazolo[3,4-c]quinolin-4-amine or a salt thereof.
 37. A method of treating viral infection, cancer, or an allergic disease, comprising administering a compound of claim 1, to a mammal in need thereof.
 38. The method of claim 38, wherein the viral infection comprises HCV infection.
 39. A dosage form suitable for administration to a mammal, comprising a compound of claim
 1. 